A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698602



Internal ID15088568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110878805..110883427hg38UCSC Ensembl
Innerchr1:111421427..111426049hg19UCSC Ensembl
Innerchr1:111222950..111227572hg18UCSC Ensembl
Innerchr1:111133469..111138091hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg384623
hg194623
hg184623
hg174623
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522939
Supporting Variants
Samples
Known GenesCD53
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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