A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613638



Internal ID16401047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14539760..14550140hg38UCSC Ensembl
Innerchr9:14539758..14550138hg19UCSC Ensembl
Innerchr9:14529758..14540138hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3810381
hg1910381
hg1810381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12571n54
Supporting Variantsnssv1128782
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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