A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv838992



Internal ID16132948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25686546..25687178hg38UCSC Ensembl
Innerchr15:25931693..25932325hg19UCSC Ensembl
Innerchr15:23482786..23483418hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38633
hg19633
hg18633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568594
Supporting Variants
Samples
Known GenesATP10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv838992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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