A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615400



Internal ID16056123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128688840..128693624hg38UCSC Ensembl
Innerchr9:131451119..131455903hg19UCSC Ensembl
Innerchr9:130490940..130495724hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384785
hg194785
hg184785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1143244, nssv1143245
Samples
Known GenesSET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615400
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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