A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614272



Internal ID16401681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38620378..38621733hg38UCSC Ensembl
Innerchr9:38620375..38621730hg19UCSC Ensembl
Innerchr9:38610375..38611730hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381356
hg191356
hg181356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12686n54
Supporting Variantsnssv1134061
Samples
Known GenesFAM201A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614272
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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