A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559774



Internal ID18858055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79557382..79574721hg38UCSC Ensembl
Innerchr16:79591279..79608618hg19UCSC Ensembl
Innerchr16:78148780..78166119hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3817340
hg1917340
hg1817340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064997
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)nssv3559774
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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