A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001080



Internal ID18743611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46804402hg38UCSC Ensembl
Innerchr3:46801805..46845892hg19UCSC Ensembl
Innerchr3:46776809..46820896hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3844088
hg1944088
hg1844088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3591044, nssv3591045
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)nsv1001080
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer