A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001789



Internal ID18744320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80484546..80539436hg38UCSC Ensembl
Innerchr3:80533696..80588586hg19UCSC Ensembl
Innerchr3:80616386..80671276hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3854891
hg1954891
hg1854891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4798n100
Supporting Variantsnssv3596232
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)nsv1001789
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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