A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590464



Internal ID18542059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4104499..4153986hg38UCSC Ensembl
Innerchr3:4146183..4195670hg19UCSC Ensembl
Innerchr3:4121183..4170670hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3849488
hg1949488
hg1849488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006386
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)nssv3590464
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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