A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690644



Internal ID15427296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53672185..53672704hg38UCSC Ensembl
Innerchr20:52288724..52289243hg19UCSC Ensembl
Innerchr20:51722131..51722650hg18UCSC Ensembl
Innerchr20:51722131..51722650hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38520
hg19520
hg18520
hg17520
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517172
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690644
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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