A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067522



Internal ID19156741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80907706..80921496hg38UCSC Ensembl
Innerchr16:80941603..80955393hg19UCSC Ensembl
Innerchr16:79499104..79512894hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3813791
hg1913791
hg1813791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3045n100
Supporting Variantsnssv3559795, nssv3559796
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)nsv1067522
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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