A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590389



Internal ID18541984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3858107..4053010hg38UCSC Ensembl
Innerchr3:3899791..4094694hg19UCSC Ensembl
Innerchr3:3874791..4069694hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38194904
hg19194904
hg18194904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997798
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)nssv3590389
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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