A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141240



Internal ID15994426
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 StatusS
Merged Variantsnsv615192
Supporting Variants
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)nssv1141240
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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