A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671693



Internal ID15408345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:65705318..65706323hg38UCSC Ensembl
Innerchr1:66171001..66172006hg19UCSC Ensembl
Innerchr1:65943589..65944594hg18UCSC Ensembl
Innerchr1:65883022..65884027hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381006
hg191006
hg181006
hg171006
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516036
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671693
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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