A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568587



Internal ID16355996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25686278..25687122hg38UCSC Ensembl
Innerchr15:25931425..25932269hg19UCSC Ensembl
Innerchr15:23482518..23483362hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38845
hg19845
hg18845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n54
Supporting Variantsnssv838866
Samples
Known GenesATP10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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