A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891742



Internal ID18839452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4974605..5101845hg38UCSC Ensembl
Outerchr10:4974605..5101845hg38UCSC Ensembl
Innerchr10:5016797..5144037hg19UCSC Ensembl
Outerchr10:5016797..5144037hg19UCSC Ensembl
Innerchr10:5006797..5134037hg18UCSC Ensembl
Outerchr10:5006797..5134037hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38127241
hg19127241
hg18127241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782995
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891742
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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