A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1013119



Internal ID16307075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171292319..171322357hg38UCSC Ensembl
Innerchr4:172213470..172243508hg19UCSC Ensembl
Innerchr4:172450045..172480083hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3830039
hg1930039
hg1830039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596172
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1013119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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