A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6390611



Internal ID9368014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144602748..144603048hg38UCSC Ensembl
chr8:145828132..145828432hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667076
Supporting Variants
SamplesNA18623
Known GenesARHGAP39
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6390611
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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