A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694757



Internal ID15431409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11037978..11056506hg38UCSC Ensembl
Innerchr20:11018626..11037154hg19UCSC Ensembl
Innerchr20:10966626..10985154hg18UCSC Ensembl
Innerchr20:10966626..10985154hg17UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3818529
hg1918529
hg1818529
hg1718529
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521990
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694757
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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