A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637068



Internal ID7023862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83226931..83236300hg38UCSC Ensembl
Innerchr15:83226933..83236298hg38UCSC Ensembl
Outerchr15:83226929..83236302hg38UCSC Ensembl
chr15:83895683..83905052hg19UCSC Ensembl
Innerchr15:83895685..83905050hg19UCSC Ensembl
Outerchr15:83895681..83905054hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg389370
hg199370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15312203, essv15312217, essv15312207, essv15312204, essv15312210, essv15312208, essv15312211, essv15312213, essv15312214, essv15312215, essv15312209, essv15312205, essv15312206, essv15312202, essv15312216, essv15312212, essv15312218
SamplesHG02610, HG03484, HG03548, HG02624, HG03464, HG02645, HG03578, HG03270, NA19095, HG02586, HG01990, HG03433, HG03419, HG03084, NA19376, HG03049, HG03470
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637068
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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