A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620788



Internal ID18919069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34768672..34828315hg38UCSC Ensembl
Innerchr4:34770294..34829937hg19UCSC Ensembl
Innerchr4:34446689..34506332hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3859644
hg1959644
hg1859644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002469
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)nssv3620788
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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