A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3485490



Internal ID19073131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5595907..5610791hg38UCSC Ensembl
Innerchr10:5637870..5652754hg19UCSC Ensembl
Innerchr10:5677876..5692760hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3814885
hg1914885
hg1814885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036798
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)nssv3485490
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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