A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051357



Internal ID18793888
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 StatusM
Merged Variantsdgv927n100
Supporting Variantsnssv3513805
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)nsv1051357
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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