A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590444



Internal ID18542039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4068629..4162139hg38UCSC Ensembl
Innerchr3:4110313..4203823hg19UCSC Ensembl
Innerchr3:4085313..4178823hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3893511
hg1993511
hg1893511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006983
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)nssv3590444
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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