A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706109



Internal ID18657704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75024700..75329039hg38UCSC Ensembl
Innerchr10:76784458..77088797hg19UCSC Ensembl
Innerchr10:76454464..76758803hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38304340
hg19304340
hg18304340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036629
Supporting Variants
Samples
Known GenesCOMTD1, DUPD1, DUSP13, KAT6B, SAMD8, 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)nssv3706109
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