A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613148



Internal ID16400557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3743938..3757758hg38UCSC Ensembl
Innerchr9:3743938..3757758hg19UCSC Ensembl
Innerchr9:3733938..3747758hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3813821
hg1913821
hg1813821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126227
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613148
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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