A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13968226



Internal ID6507908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126967806..126984836hg38UCSC Ensembl
chr10:128766065..128783100hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3817031
hg1917036
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624868
Supporting Variants
SamplesNA20535
Known GenesDOCK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13968226
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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