A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5459724



Internal ID8437127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59193328..59193721hg38UCSC Ensembl
chr10:60953088..60953481hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676927
Supporting Variants
SamplesNA18989
Known GenesPHYHIPL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5459724
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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