A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663850



Internal ID15400502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52706086..52733495hg38UCSC Ensembl
Innerchr15:52998283..53025692hg19UCSC Ensembl
Innerchr15:50785575..50812984hg18UCSC Ensembl
Innerchr15:50785575..50812984hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3827410
hg1927410
hg1827410
hg1727410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515534
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663850
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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