A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017038



Internal ID16310994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178184384..178414107hg38UCSC Ensembl
Innerchr4:179105538..179335261hg19UCSC Ensembl
Innerchr4:179342532..179572255hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38229724
hg19229724
hg18229724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596271
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)nssv1017038
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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