A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5977906



Internal ID8955309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43887894..43888638hg38UCSC Ensembl
chr10:44383342..44384086hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667357
Supporting Variants
SamplesNA19383
Known GenesLINC00840
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5977906
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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