A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891752



Internal ID18839462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7698285..7742961hg38UCSC Ensembl
Outerchr10:7697592..7743053hg38UCSC Ensembl
Innerchr10:7740248..7784924hg19UCSC Ensembl
Outerchr10:7739555..7785016hg19UCSC Ensembl
Innerchr10:7780254..7824930hg18UCSC Ensembl
Outerchr10:7779561..7825022hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3845462
hg1945462
hg1845462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787796, essv25788350
Samples
Known GenesITIH2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891752
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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