A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568597



Internal ID16356006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25686696..25687843hg38UCSC Ensembl
Innerchr15:25931843..25932990hg19UCSC Ensembl
Innerchr15:23482936..23484083hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381148
hg191148
hg181148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4393n54
Supporting Variantsnssv839147, nssv839148
Samples
Known GenesATP10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568597
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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