A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697432



Internal ID15434084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109184800..109196449hg38UCSC Ensembl
Innerchr1:109727422..109739071hg19UCSC Ensembl
Innerchr1:109528945..109540594hg18UCSC Ensembl
Innerchr1:109439464..109451113hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3811650
hg1911650
hg1811650
hg1711650
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520456
Supporting Variants
Samples
Known GenesKIAA1324
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697432
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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