Variant Details

Variant: esv3356338

Internal ID

15203318

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr13:78010525..78010535	hg38	UCSC Ensembl
Inner	chr13:78010517..78010543	hg38	UCSC Ensembl
Outer	chr13:78010504..78010553	hg38	UCSC Ensembl
	chr13:78584660..78584670	hg19	UCSC Ensembl
Inner	chr13:78584652..78584678	hg19	UCSC Ensembl
Outer	chr13:78584639..78584688	hg19	UCSC Ensembl
	chr13:77482661..77482671	hg18	UCSC Ensembl
Inner	chr13:77482679..77482653	hg18	UCSC Ensembl
Outer	chr13:77482640..77482689	hg18	UCSC Ensembl

Cytoband

13q22.3

Allele length

Assembly	Allele length
hg38	289
hg19	289
hg18	289

Variant Type

CNV insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv8962157, essv8962107, essv8962180, essv8962165, essv8962083, essv8962105, essv8962090, essv8962178, essv8962138, essv8962120, essv8962151, essv8962116, essv8962092, essv8962089, essv8962118, essv8962100, essv8962087, essv8962141, essv8962099, essv8962127, essv8962156, essv8962133, essv8962117, essv8962086, essv8962176, essv8962093, essv8962123, essv8962110, essv8962088, essv8962097, essv8962131, essv8962154, essv8962175, essv8962171, essv8962104, essv8962085, essv8962096, essv8962084, essv8962122, essv8962129, essv8962143, essv8962128, essv8962112, essv8962098, essv8962125, essv8962095, essv8962172, essv8962135, essv8962152, essv8962119, essv8962144, essv8962182, essv8962166, essv8962142, essv8962124, essv8962139, essv8962167, essv8962174, essv8962140, essv8962146, essv8962134, essv8962155, essv8962158, essv8962179, essv8962161, essv8962121, essv8962108, essv8962147, essv8962162, essv8962164, essv8962169, essv8962111, essv8962163, essv8962130, essv8962177, essv8962153, essv8962145, essv8962094, essv8962106, essv8962160, essv8962103, essv8962132, essv8962149, essv8962109, essv8962173, essv8962168, essv8962101, essv8962150, essv8962136

Samples

NA18502, NA12717, NA11830, NA11829, NA18592, NA18508, NA10851, NA12414, NA18980, NA18561, NA11920, NA11931, NA18603, NA12751, NA12004, NA18504, NA18959, NA18870, NA18526, NA12750, NA12155, NA07346, NA19005, NA18940, NA18519, NA18960, NA18942, NA18916, NA11992, NA11918, NA07347, NA18582, NA18571, NA12287, NA18964, NA18949, NA12761, NA11994, NA19172, NA12828, NA18973, NA11993, NA11831, NA10847, NA18951, NA12489, NA12003, NA18956, NA18871, NA18572, NA18948, NA19114, NA11894, NA12249, NA18853, NA19099, NA18555, NA18523, NA18570, NA18858, NA12043, NA18953, NA18542, NA12716, NA18909, NA11881, NA19108, NA18961, NA19147, NA18517, NA18564, NA07051, NA18943, NA07037, NA12763, NA18501, NA12749, NA19093, NA18609, NA19102, NA18552, NA19129, NA12006, NA18511, NA07000, NA12154, NA18562, NA12776, NA18965

Known Genes

Method

Sequencing

Analysis

Platform

Illumina

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3356338

Frequency

Sample Size	185
Observed Gain	89
Observed Loss	0
Observed Complex	0
Frequency	n/a