A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008998



Internal ID18751529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..160351hg38UCSC Ensembl
Innerchr3:60333..202034hg19UCSC Ensembl
Innerchr3:35333..177034hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38141697
hg19141702
hg18141702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4606n100
Supporting Variantsnssv3590209, nssv3590208
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)nsv1008998
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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