A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698598



Internal ID15088564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:70421500..70422418hg38UCSC Ensembl
Innerchr1:70887183..70888101hg19UCSC Ensembl
Innerchr1:70659771..70660689hg18UCSC Ensembl
Innerchr1:70599204..70600122hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38919
hg19919
hg18919
hg17919
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522935
Supporting Variants
Samples
Known GenesCTH
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698598
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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