A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613266



Internal ID16400675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7588854..7901308hg38UCSC Ensembl
Innerchr9:7588854..7901308hg19UCSC Ensembl
Innerchr9:7578854..7891308hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38312455
hg19312455
hg18312455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156227
Samples1780862339_A
Known GenesTMEM261
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613266
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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