A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638007



Internal ID7024793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14405864..14411282hg38UCSC Ensembl
Innerchr16:14405901..14411246hg38UCSC Ensembl
Outerchr16:14405828..14411319hg38UCSC Ensembl
chr16:14499721..14505139hg19UCSC Ensembl
Innerchr16:14499758..14505103hg19UCSC Ensembl
Outerchr16:14499685..14505176hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385419
hg195419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15379360, essv15379367, essv15379370, essv15379372, essv15379371, essv15379362, essv15379361, essv15379364, essv15379363, essv15379366, essv15379368, essv15379365, essv15379369, essv15379359, essv15379358, essv15379357
SamplesHG02339, NA18507, NA18881, HG03130, HG02895, HG01495, NA19189, NA18934, HG02497, NA18907, HG03571, HG02314, HG03473, HG01342, HG02558, NA18505
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638007
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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