A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999347



Internal ID19158883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95113446..95458906hg38UCSC Ensembl
Innerchr3:94832290..95177750hg19UCSC Ensembl
Innerchr3:96314980..96660440hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38345461
hg19345461
hg18345461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4815n100
Supporting Variantsnssv3735178
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)nsv999347
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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