A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038809



Internal ID19128028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1893193..1943725hg38UCSC Ensembl
Innerchr10:1935387..1985919hg19UCSC Ensembl
Innerchr10:1925387..1975919hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3850533
hg1950533
hg1850533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv657n100
Supporting Variantsnssv3707664
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)nsv1038809
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