A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15276122



Internal ID4352638
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636789
Supporting Variants
SamplesHG03888
Known GenesC15orf61, IQCH-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15276122
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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