A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589477



Internal ID18887758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22069558..22214639hg38UCSC Ensembl
Innerchr3:22111050..22256131hg19UCSC Ensembl
Innerchr3:22086054..22231135hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38145082
hg19145082
hg18145082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009816
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)nssv3589477
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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