A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701010



Internal ID15090976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23030831..23040960hg38UCSC Ensembl
Innerchr20:23011468..23021597hg19UCSC Ensembl
Innerchr20:22959468..22969597hg18UCSC Ensembl
Innerchr20:22959468..22969597hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3810130
hg1910130
hg1810130
hg1710130
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524981
Supporting Variants
Samples
Known GenesSSTR4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701010
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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