A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584721



Internal ID18883002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30185664..30295239hg38UCSC Ensembl
Innerchr20:29420340..29529915hg19UCSC Ensembl
Innerchr20:28034001..28143576hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg38109576
hg19109576
hg18109576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056924
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584721
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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