A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6123677



Internal ID9600451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93225187..93231374hg38UCSC Ensembl
chr8:94237416..94243603hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg386188
hg196188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677227
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6123677
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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