A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037772



Internal ID18780303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133263092..133403671hg38UCSC Ensembl
Innerchr10:135076596..135217175hg19UCSC Ensembl
Innerchr10:134926587..135067165hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38140580
hg19140580
hg18140579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706262
Samples
Known GenesADAM8, CALY, ECHS1, FUOM, MIR3944, MTG1, PAOX, PRAP1, TUBGCP2, ZNF511
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037772
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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