A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589478



Internal ID18887759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22139669..22166209hg38UCSC Ensembl
Innerchr3:22181161..22207701hg19UCSC Ensembl
Innerchr3:22156165..22182705hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3826541
hg1926541
hg1826541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011688
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)nssv3589478
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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