A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552589



Internal ID15993312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133257500..133563944hg38UCSC Ensembl
Innerchr10:135071004..135377448hg19UCSC Ensembl
Innerchr10:134920995..135227438hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38306445
hg19306445
hg18306444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv762203
Samples
Known GenesADAM8, CALY, CYP2E1, ECHS1, FUOM, MIR3944, MTG1, PAOX, PRAP1, SCART1, SPRN, SYCE1, TUBGCP2, ZNF511
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552589
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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