A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613704



Internal ID16401113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17583312..17633234hg38UCSC Ensembl
Innerchr9:17583310..17633232hg19UCSC Ensembl
Innerchr9:17573310..17623232hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3849923
hg1949923
hg1849923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12581n54
Supporting Variantsnssv1129333, nssv1129332, nssv1129334, nssv1156262, nssv1156261, nssv1129335
SamplesHGDP00539, 1780862003_A
Known GenesSH3GL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613704
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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