A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513805



Internal ID18465400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75024700..75325170hg38UCSC Ensembl
Innerchr10:76784458..77084928hg19UCSC Ensembl
Innerchr10:76454464..76754934hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38300471
hg19300471
hg18300471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051357
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)nssv3513805
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