A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13860901



Internal ID3454333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71869436..71876066hg38UCSC Ensembl
Innerchr10:71869936..71875566hg38UCSC Ensembl
Outerchr10:71868436..71877066hg38UCSC Ensembl
chr10:73629194..73635824hg19UCSC Ensembl
Innerchr10:73629694..73635324hg19UCSC Ensembl
Outerchr10:73628194..73636824hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386631
hg196631
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623781
Supporting Variants
SamplesHG03079
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13860901
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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