A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036634



Internal ID18779165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6770897..6802174hg38UCSC Ensembl
Innerchr16:6820898..6852175hg19UCSC Ensembl
Innerchr16:6760899..6792176hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3831278
hg1931278
hg1831278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718853, nssv3557053
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036634
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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