A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036629



Internal ID18779160
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 StatusM
Merged Variantsdgv927n100
Supporting Variantsnssv3706109
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)nsv1036629
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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