A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568589



Internal ID16355998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25686329..25687843hg38UCSC Ensembl
Innerchr15:25931476..25932990hg19UCSC Ensembl
Innerchr15:23482569..23484083hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381515
hg191515
hg181515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4393n54
Supporting Variantsnssv838901
Samples
Known GenesATP10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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