A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764082



Internal ID5213908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42689080..42751910hg38UCSC Ensembl
chr10:43184528..43247358hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3862831
hg1962831
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623023
Supporting Variants
SamplesNA18620
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764082
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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