Variant Details

Variant: esv3637843

Internal ID

6677943

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr16:8732186..8733864	hg38	UCSC Ensembl
Inner	chr16:8732187..8733863	hg38	UCSC Ensembl
Outer	chr16:8732185..8733865	hg38	UCSC Ensembl
	chr16:8826043..8827721	hg19	UCSC Ensembl
Inner	chr16:8826044..8827720	hg19	UCSC Ensembl
Outer	chr16:8826042..8827722	hg19	UCSC Ensembl

Cytoband

16p13.2

Allele length

Assembly	Allele length
hg38	1679
hg19	1679

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15371986, essv15371960, essv15371994, essv15371930, essv15371951, essv15371992, essv15371931, essv15371933, essv15371957, essv15371936, essv15371922, essv15371972, essv15371969, essv15371973, essv15371981, essv15371970, essv15371947, essv15371979, essv15371965, essv15371993, essv15371938, essv15371924, essv15371939, essv15371988, essv15371925, essv15371984, essv15371964, essv15371934, essv15371937, essv15371977, essv15371963, essv15371943, essv15371975, essv15371980, essv15371946, essv15371983, essv15371929, essv15371989, essv15371990, essv15371952, essv15371945, essv15371932, essv15371968, essv15371978, essv15371942, essv15371944, essv15371961, essv15371976, essv15371967, essv15371956, essv15371927, essv15371953, essv15371940, essv15371935, essv15371955, essv15371985, essv15371948, essv15371954, essv15371974, essv15371950, essv15371949, essv15371987, essv15371971, essv15371959, essv15371991, essv15371996, essv15371966, essv15371995, essv15371923, essv15371926, essv15371982, essv15371928, essv15371958, essv15371962, essv15371941

Samples

HG02610, HG03163, HG02419, HG02798, NA19020, NA19350, NA20321, NA18486, HG03521, NA20294, HG03455, HG02624, HG01971, HG03139, HG03372, NA18510, HG03095, NA19171, NA18519, HG03086, HG02952, NA20320, NA19119, NA19904, HG02703, NA19137, NA19901, HG02502, NA19189, NA18520, HG03114, NA19027, HG03270, NA19908, HG03132, NA19984, HG02449, NA19913, NA18516, HG02307, NA18871, HG02976, HG02537, HG01889, HG03124, HG01049, HG03472, NA19461, HG02577, NA19113, NA18853, NA20282, HG03046, NA19452, HG01890, NA19095, HG01956, HG02813, HG02255, NA19206, NA19108, NA18517, HG01894, NA19380, NA19144, NA19323, NA19143, HG03313, HG02938, HG03060, HG02013, NA19711, HG01883, HG03118, NA19214

Known Genes

ABAT

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3637843

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	75
Observed Complex	0
Frequency	n/a