A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591632



Internal ID18543227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4224848..4259411hg38UCSC Ensembl
Innerchr3:4266532..4301095hg19UCSC Ensembl
Innerchr3:4241532..4276095hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3834564
hg1934564
hg1834564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999405
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)nssv3591632
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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