A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063641



Internal ID19152860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79557382..79580271hg38UCSC Ensembl
Innerchr16:79591279..79614168hg19UCSC Ensembl
Innerchr16:78148780..78171669hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3822890
hg1922890
hg1822890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3041n100
Supporting Variantsnssv3559777
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)nsv1063641
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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