A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590467



Internal ID18542062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4104499..4166100hg38UCSC Ensembl
Innerchr3:4146183..4207784hg19UCSC Ensembl
Innerchr3:4121183..4182784hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3861602
hg1961602
hg1861602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012735
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)nssv3590467
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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