A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13856346



Internal ID897119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69685218..69689342hg38UCSC Ensembl
chr10:71444974..71449098hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384125
hg194125
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623754
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13856346
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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