A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669332



Internal ID15405984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72555560..72618538hg38UCSC Ensembl
Innerchr1:73021243..73084221hg19UCSC Ensembl
Innerchr1:72793831..72856809hg18UCSC Ensembl
Innerchr1:72733264..72796242hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3862979
hg1962979
hg1862979
hg1762979
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516582
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669332
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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