A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615914



Internal ID16056637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135667116..135699384hg38UCSC Ensembl
Innerchr9:138558962..138591230hg19UCSC Ensembl
Innerchr9:137698783..137731051hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3832269
hg1932269
hg1832269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12990n54
Supporting Variantsnssv1148244
Samples
Known GenesSOHLH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615914
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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