A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584656



Internal ID18882937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22064367..22168160hg38UCSC Ensembl
Innerchr20:22045005..22148798hg19UCSC Ensembl
Innerchr20:21993005..22096798hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38103794
hg19103794
hg18103794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058614
Supporting Variants
Samples
Known GenesLOC100270679
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584656
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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