A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683459



Internal ID15420111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20494784..20562084hg38UCSC Ensembl
Innerchr10:20783713..20851013hg19UCSC Ensembl
Innerchr10:20823719..20891019hg18UCSC Ensembl
Innerchr10:20823719..20891019hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3867301
hg1967301
hg1867301
hg1767301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516763
Supporting Variants
Samples
Known GenesMIR4675
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683459
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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