A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589448



Internal ID18887729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21943888..21966605hg38UCSC Ensembl
Innerchr3:21985380..22008097hg19UCSC Ensembl
Innerchr3:21960384..21983101hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3822718
hg1922718
hg1822718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014467
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)nssv3589448
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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