A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614808



Internal ID16402217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88506971..88535071hg38UCSC Ensembl
Innerchr9:91121886..91149986hg19UCSC Ensembl
Innerchr9:90311706..90339806hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3828101
hg1928101
hg1828101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139149
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614808
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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