A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692106



Internal ID15428758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101900584..101965078hg38UCSC Ensembl
Innerchr1:102366140..102430634hg19UCSC Ensembl
Innerchr1:102138728..102203222hg18UCSC Ensembl
Innerchr1:102078161..102142655hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3864495
hg1964495
hg1864495
hg1764495
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)nssv692106
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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