A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622457



Internal ID7009316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15865992..15872303hg38UCSC Ensembl
Innerchr10:15865992..15872303hg38UCSC Ensembl
Outerchr10:15865492..15872803hg38UCSC Ensembl
chr10:15907991..15914302hg19UCSC Ensembl
Innerchr10:15907991..15914302hg19UCSC Ensembl
Outerchr10:15907491..15914802hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386312
hg196312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704551, essv13704552
SamplesNA19031, NA19338
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622457
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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