A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998469



Internal ID19158005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11883204..11912374hg38UCSC Ensembl
Innerchr3:11924678..11953848hg19UCSC Ensembl
Innerchr3:11899678..11928848hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3829171
hg1929171
hg1829171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4682n100
Supporting Variantsnssv3591949
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)nsv998469
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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