A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515935



Internal ID15442992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5778431..5827876hg38UCSC Ensembl
Innerchr10:5820394..5869839hg19UCSC Ensembl
Innerchr10:5860400..5909845hg18UCSC Ensembl
Innerchr10:5860400..5909845hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3849446
hg1949446
hg1849446
hg1749446
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661133, nssv668657, nssv665378
Samples
Known GenesGDI2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515935
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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