A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613128



Internal ID16400537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2253678..2419538hg38UCSC Ensembl
Innerchr9:2253678..2419538hg19UCSC Ensembl
Innerchr9:2243678..2409538hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38165861
hg19165861
hg18165861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126216
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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