A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064997



Internal ID19154216
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 StatusM
Merged Variantsdgv3041n100
Supporting Variantsnssv3559774, nssv3559775
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)nsv1064997
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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