A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704809



Internal ID15441461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53694915..53698772hg38UCSC Ensembl
Innerchr20:52311454..52315311hg19UCSC Ensembl
Innerchr20:51744861..51748718hg18UCSC Ensembl
Innerchr20:51744861..51748718hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg383858
hg193858
hg183858
hg173858
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517748
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704809
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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