A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998095



Internal ID18810945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24337..160351hg38UCSC Ensembl
Innerchr3:66011..202034hg19UCSC Ensembl
Innerchr3:41011..177034hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38136015
hg19136024
hg18136024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4606n100
Supporting Variantsnssv3590232
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)nsv998095
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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