A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699103



Internal ID15089069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:92465706..92599266hg38UCSC Ensembl
Innerchr1:92931263..93064823hg19UCSC Ensembl
Innerchr1:92703851..92837411hg18UCSC Ensembl
Innerchr1:92643284..92776844hg17UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38133561
hg19133561
hg18133561
hg17133561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523354
Supporting Variants
Samples
Known GenesEVI5, GFI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699103
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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