A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891891



Internal ID18839601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119615669..119652348hg38UCSC Ensembl
Outerchr10:119615669..119657099hg38UCSC Ensembl
Innerchr10:121375181..121411860hg19UCSC Ensembl
Outerchr10:121375181..121416611hg19UCSC Ensembl
Innerchr10:121365171..121401850hg18UCSC Ensembl
Outerchr10:121365171..121406601hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3841431
hg1941431
hg1841431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788020, essv25788130
Samples
Known GenesBAG3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891891
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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