A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13851059



Internal ID5979713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68422616..68427983hg38UCSC Ensembl
Innerchr10:68422634..68427966hg38UCSC Ensembl
Outerchr10:68422599..68428001hg38UCSC Ensembl
chr10:70182373..70187740hg19UCSC Ensembl
Innerchr10:70182391..70187723hg19UCSC Ensembl
Outerchr10:70182356..70187758hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg385368
hg195368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623715
Supporting Variants
SamplesNA19385
Known GenesDNA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13851059
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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