A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529008



Internal ID15109615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68493946..68536147hg38UCSC Ensembl
Innerchr15:68786285..68828486hg19UCSC Ensembl
Innerchr15:66573339..66615540hg18UCSC Ensembl
Innerchr15:66573339..66615540hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3842202
hg1942202
hg1842202
hg1742202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705718
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529008
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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