A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521813



Internal ID15449106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119046720..119076825hg38UCSC Ensembl
Innerchr1:119589343..119619448hg19UCSC Ensembl
Innerchr1:119390866..119420971hg18UCSC Ensembl
Innerchr1:119301385..119331490hg17UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3830106
hg1930106
hg1830106
hg1730106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694585
Samples
Known GenesWARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521813
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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