A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636142



Internal ID18934423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156481370..156583441hg38UCSC Ensembl
Innerchr4:157402522..157504593hg19UCSC Ensembl
Innerchr4:157621972..157724043hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38102072
hg19102072
hg18102072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026528
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636142
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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