A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593759



Internal ID18545354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46827326hg38UCSC Ensembl
Innerchr3:46801805..46868816hg19UCSC Ensembl
Innerchr3:46776809..46843820hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3867012
hg1967012
hg1867012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999521
Supporting Variants
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)nssv3593759
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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