A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13855085



Internal ID1548400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69401159..69402210hg38UCSC Ensembl
Innerchr10:69401171..69402198hg38UCSC Ensembl
Outerchr10:69401147..69402222hg38UCSC Ensembl
chr10:71160915..71161966hg19UCSC Ensembl
Innerchr10:71160927..71161954hg19UCSC Ensembl
Outerchr10:71160903..71161978hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623743
Supporting Variants
SamplesHG01432
Known GenesHK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13855085
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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