A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668657



Internal ID15405309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5778431..5815021hg38UCSC Ensembl
Innerchr10:5820394..5856984hg19UCSC Ensembl
Innerchr10:5860400..5896990hg18UCSC Ensembl
Innerchr10:5860400..5896990hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3836591
hg1936591
hg1836591
hg1736591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515935
Supporting Variants
Samples
Known GenesGDI2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668657
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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