Variant Details

Variant: esv3436267

Internal ID

15283220

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr6:13718233..13718246	hg38	UCSC Ensembl
Inner	chr6:13718223..13718254	hg38	UCSC Ensembl
Outer	chr6:13718210..13718267	hg38	UCSC Ensembl
	chr6:13718465..13718478	hg19	UCSC Ensembl
Inner	chr6:13718455..13718486	hg19	UCSC Ensembl
Outer	chr6:13718442..13718499	hg19	UCSC Ensembl
	chr6:13826444..13826457	hg18	UCSC Ensembl
Inner	chr6:13826465..13826434	hg18	UCSC Ensembl
Outer	chr6:13826421..13826478	hg18	UCSC Ensembl

Cytoband

6p23

Allele length

Assembly	Allele length
hg38	270
hg19	270
hg18	270

Variant Type

CNV insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv8927937, essv8928013, essv8927988, essv8927945, essv8927961, essv8927940, essv8928004, essv8927946, essv8928015, essv8927951, essv8928006, essv8928012, essv8927982, essv8928022, essv8927996, essv8927979, essv8927956, essv8927939, essv8927965, essv8927992, essv8927989, essv8927984, essv8927987, essv8927944, essv8927966, essv8928009, essv8927995, essv8927957, essv8927983, essv8928011, essv8927977, essv8928017, essv8927981, essv8927935, essv8928005, essv8928008, essv8927994, essv8927974, essv8928007, essv8928001, essv8927997, essv8927973, essv8928021, essv8927968, essv8927999, essv8927955, essv8927985, essv8927975, essv8927963, essv8927964, essv8927986, essv8927998, essv8927978, essv8927962, essv8927967, essv8927990, essv8927949, essv8928000, essv8927942, essv8928020, essv8927954, essv8928016, essv8928019, essv8927931, essv8927938, essv8927952, essv8928018, essv8927943, essv8927948, essv8927993, essv8927933, essv8927950, essv8927932, essv8927959, essv8927970, essv8927976, essv8927953, essv8927934, essv8927972, essv8927941, essv8928010, essv8927971, essv8927960

Samples

NA18502, NA12717, NA11995, NA11829, NA18861, NA18592, NA18508, NA10851, NA12414, NA18980, NA18561, NA11931, NA18603, NA12045, NA12004, NA18504, NA18870, NA18526, NA18510, NA12155, NA07357, NA07346, NA18563, NA19005, NA18550, NA18519, NA18489, NA18942, NA18916, NA11918, NA07347, NA18582, NA19138, NA18964, NA18949, NA12761, NA12044, NA11994, NA19172, NA18520, NA12828, NA11831, NA18579, NA18871, NA18907, NA18537, NA18566, NA18573, NA18499, NA18856, NA18532, NA19099, NA19257, NA18555, NA19225, NA12144, NA18523, NA18858, NA18593, NA18576, NA18608, NA18542, NA12716, NA18909, NA11881, NA19108, NA18961, NA19147, NA18517, NA18564, NA18943, NA07037, NA06986, NA18501, NA12749, NA19093, NA18505, NA19129, NA12006, NA18522, NA12776, NA18965, NA18577

Known Genes

Method

Sequencing

Analysis

Platform

Illumina

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3436267

Frequency

Sample Size	185
Observed Gain	83
Observed Loss	0
Observed Complex	0
Frequency	n/a