A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704808



Internal ID15441460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2441096..2448576hg38UCSC Ensembl
Innerchr20:2421742..2429222hg19UCSC Ensembl
Innerchr20:2369742..2377222hg18UCSC Ensembl
Innerchr20:2369742..2377222hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387481
hg197481
hg187481
hg177481
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528245
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704808
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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