A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614273



Internal ID16401682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38620715..38621733hg38UCSC Ensembl
Innerchr9:38620712..38621730hg19UCSC Ensembl
Innerchr9:38610712..38611730hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381019
hg191019
hg181019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12686n54
Supporting Variantsnssv1134062
Samples
Known GenesFAM201A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614273
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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