A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5956377



Internal ID8881518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43599977..43600158hg38UCSC Ensembl
chr10:44095425..44095606hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664354
Supporting Variants
SamplesHG00331
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5956377
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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