A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614658



Internal ID16055381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74454955..74539535hg38UCSC Ensembl
Innerchr9:77069871..77154451hg19UCSC Ensembl
Innerchr9:76259691..76344271hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3884581
hg1984581
hg1884581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137323
Samples
Known GenesMIR6130, RORB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614658
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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