A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13756622



Internal ID1799753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36506881..36550201hg38UCSC Ensembl
chr10:36795809..36839129hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3843321
hg1943321
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622925
Supporting Variants
SamplesHG01678
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13756622
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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