A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065656



Internal ID19154875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33535645..34035419hg38UCSC Ensembl
Innerchr16:33338112..33837886hg19UCSC Ensembl
Innerchr16:33245613..33745387hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38499775
hg19499775
hg18499775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2915n100
Supporting Variantsnssv3717444, nssv3553273, nssv3553274
Samples
Known GenesRNU6-76P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065656
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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