A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998594



Internal ID18811444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..103149hg38UCSC Ensembl
Innerchr3:60333..144832hg19UCSC Ensembl
Innerchr3:35333..119832hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3884495
hg1984500
hg1884500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590186
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)nsv998594
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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