A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6018694



Internal ID9142239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39374555..39529709hg38UCSC Ensembl
chr8:39232074..39387228hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155155
hg19155155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666583
Supporting Variants
SamplesHG01188
Known GenesADAM3A, ADAM5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6018694
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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