A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006983



Internal ID18749514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4068629..4162139hg38UCSC Ensembl
Innerchr3:4110313..4203823hg19UCSC Ensembl
Innerchr3:4085313..4178823hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3893511
hg1993511
hg1893511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4648n100
Supporting Variantsnssv3590444
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)nsv1006983
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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