A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981589



Internal ID12625681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133408615..133620615hg38UCSC Ensembl
Innerchr10:135222119..135434119hg19UCSC Ensembl
Innerchr10:135072109..135284109hg18UCSC Ensembl
Innerchr10:135111000..135323000hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38212001
hg19212001
hg18212001
hg17212001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750862
Supporting Variants
SamplesBEC_303
Known GenesCYP2E1, MTG1, SCART1, SPRN, SPRNP1, SYCE1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981589
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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