A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615192



Internal ID16402601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111624319..111661153hg38UCSC Ensembl
Innerchr9:114386599..114423433hg19UCSC Ensembl
Innerchr9:113426420..113463254hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3836835
hg1936835
hg1836835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141240
Samples
Known GenesDNAJC25, DNAJC25-GNG10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615192
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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