A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636789



Internal ID7023583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67514940..67521624hg38UCSC Ensembl
Innerchr15:67514940..67521624hg38UCSC Ensembl
Outerchr15:67514855..67521778hg38UCSC Ensembl
chr15:67807278..67813962hg19UCSC Ensembl
Innerchr15:67807278..67813962hg19UCSC Ensembl
Outerchr15:67807193..67814116hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386685
hg196685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15276122, essv15276123, essv15276121
SamplesHG03722, HG03888, HG03955
Known GenesC15orf61, IQCH-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636789
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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