A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515939



Internal ID15096546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65389463..65401218hg38UCSC Ensembl
Innerchr15:65681801..65693556hg19UCSC Ensembl
Innerchr15:63468854..63480609hg18UCSC Ensembl
Innerchr15:63468854..63480609hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3811756
hg1911756
hg1811756
hg1711756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665385, nssv696784, nssv680834, nssv683184, nssv674873, nssv690757, nssv675695, nssv668508, nssv655114, nssv672372, nssv676076, nssv654691, nssv668723, nssv673139, nssv685773
Samples
Known GenesIGDCC4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515939
Frequency
Sample Size2026
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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