A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624589



Internal ID7011442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112972067..112973857hg38UCSC Ensembl
Innerchr10:112972117..112973807hg38UCSC Ensembl
Outerchr10:112972001..112973923hg38UCSC Ensembl
chr10:114731826..114733616hg19UCSC Ensembl
Innerchr10:114731876..114733566hg19UCSC Ensembl
Outerchr10:114731760..114733682hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381791
hg191791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13939566
SamplesHG01685
Known GenesTCF7L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624589
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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