A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525633



Internal ID15452926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:223460250..223465127hg38UCSC Ensembl
Innerchr2:224324968..224329845hg19UCSC Ensembl
Innerchr2:224033212..224038089hg18UCSC Ensembl
Innerchr2:224150473..224155350hg17UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg384878
hg194878
hg184878
hg174878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701786
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525633
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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