A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730376



Internal ID19028657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:361224..384103hg38UCSC Ensembl
Innerchr20:341868..364747hg19UCSC Ensembl
Innerchr20:289868..312747hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3822880
hg1922880
hg1822880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065287
Supporting Variants
Samples
Known GenesTRIB3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3730376
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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