A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619911



Internal ID18918192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22043744..22067050hg38UCSC Ensembl
Innerchr4:22045367..22068673hg19UCSC Ensembl
Innerchr4:21654465..21677771hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3823307
hg1923307
hg1823307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014170
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)nssv3619911
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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