A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697559



Internal ID15434211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101937189..101944959hg38UCSC Ensembl
Innerchr1:102402745..102410515hg19UCSC Ensembl
Innerchr1:102175333..102183103hg18UCSC Ensembl
Innerchr1:102114766..102122536hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg387771
hg197771
hg187771
hg177771
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520768
Supporting Variants
Samples
Known GenesMIR548AI, OLFM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697559
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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