A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516384



Internal ID15096991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28920744..28996217hg38UCSC Ensembl
Innerchr15:29212947..29288420hg19UCSC Ensembl
Innerchr15:27000239..27075712hg18UCSC Ensembl
Innerchr15:27000239..27075712hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3875474
hg1975474
hg1875474
hg1775474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667939, nssv654752, nssv676684, nssv655931
Samples
Known GenesAPBA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516384
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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