A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590396



Internal ID18888677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3918349..3933034hg38UCSC Ensembl
Innerchr3:3960033..3974718hg19UCSC Ensembl
Innerchr3:3935033..3949718hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3814686
hg1914686
hg1814686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006862
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)nssv3590396
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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