A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053530



Internal ID18796061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75224182..75323491hg38UCSC Ensembl
Innerchr10:76983940..77083249hg19UCSC Ensembl
Innerchr10:76653946..76753255hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3899310
hg1999310
hg1899310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv928n100
Supporting Variantsnssv3522567
Samples
Known GenesCOMTD1, VDAC2, ZNF503-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053530
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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