A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001582



Internal ID19090799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46751875..46806114hg38UCSC Ensembl
Innerchr3:46793365..46847604hg19UCSC Ensembl
Innerchr3:46768369..46822608hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3854240
hg1954240
hg1854240
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4733n100
Supporting Variantsnssv3590927, nssv3590925, nssv3590922, nssv3590923, nssv3590924, nssv3590928, nssv3590921, nssv3739712, nssv3590931, nssv3590929, nssv3590930, nssv3590926, nssv3590932
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)nsv1001582
Frequency
Sample Size11257
Observed Gain1
Observed Loss12
Observed Complex0
Frequencyn/a


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