A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008543



Internal ID19097760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42331147..42359541hg38UCSC Ensembl
Innerchr3:42372639..42401033hg19UCSC Ensembl
Innerchr3:42347643..42376037hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3828395
hg1928395
hg1828395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589729
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)nsv1008543
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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