A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999539



Internal ID19159076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90219616..90436800hg38UCSC Ensembl
Innerchr3:90268766..90485950hg19UCSC Ensembl
Innerchr3:90351456..90568640hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38217185
hg19217185
hg18217185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4812n100
Supporting Variantsnssv3603284, nssv3603283
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)nsv999539
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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