A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568596



Internal ID16356005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25686645..25687178hg38UCSC Ensembl
Innerchr15:25931792..25932325hg19UCSC Ensembl
Innerchr15:23482885..23483418hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38534
hg19534
hg18534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4394n54
Supporting Variantsnssv839146
Samples
Known GenesATP10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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