A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623742



Internal ID7010598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69325941..69327101hg38UCSC Ensembl
Innerchr10:69325970..69327073hg38UCSC Ensembl
Outerchr10:69325913..69327130hg38UCSC Ensembl
chr10:71085697..71086857hg19UCSC Ensembl
Innerchr10:71085726..71086829hg19UCSC Ensembl
Outerchr10:71085669..71086886hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13855080, essv13855084, essv13855079, essv13855083, essv13855081, essv13855082
SamplesHG02688, HG02775, HG02725, HG02684, HG03019, HG03684
Known GenesHK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623742
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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