A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13855000



Internal ID4119123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69294191..69311776hg38UCSC Ensembl
chr10:71053947..71071532hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3817586
hg1917586
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623740
Supporting Variants
SamplesHG03738
Known GenesHK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13855000
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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