A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv651879



Internal ID15041845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:68116157..68116291hg38UCSC Ensembl
Innerchr1:68581840..68581974hg19UCSC Ensembl
Innerchr1:68354428..68354562hg18UCSC Ensembl
Innerchr1:68293861..68293995hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38135
hg19135
hg18135
hg17135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517355
Supporting Variants
Samples
Known GenesGNG12-AS1, WLS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv651879
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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