A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040422



Internal ID19129641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5672667hg38UCSC Ensembl
Innerchr10:5665458..5714630hg19UCSC Ensembl
Innerchr10:5705464..5754636hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3849173
hg1949173
hg1849173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv665n100
Supporting Variantsnssv3488699
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)nsv1040422
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