A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1010282



Internal ID16304238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161093011..161169603hg38UCSC Ensembl
Innerchr4:162014163..162090755hg19UCSC Ensembl
Innerchr4:162233613..162310205hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3876593
hg1976593
hg1876593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595942
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)nssv1010282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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