A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3498882



Internal ID19086523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5678549hg38UCSC Ensembl
Innerchr10:5665458..5720512hg19UCSC Ensembl
Innerchr10:5705464..5760518hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3855055
hg1955055
hg1855055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039650
Supporting Variants
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3498882
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