A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997648



Internal ID18810498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..164435hg38UCSC Ensembl
Innerchr3:60333..206118hg19UCSC Ensembl
Innerchr3:35333..181118hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38145781
hg19145786
hg18145786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4606n100
Supporting Variantsnssv3590210
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)nsv997648
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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