A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6441610



Internal ID9899349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139111723..139114810hg38UCSC Ensembl
Outerchr8:139111686..139114860hg38UCSC Ensembl
Innerchr8:140123966..140127053hg19UCSC Ensembl
Outerchr8:140123929..140127103hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383175
hg193175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669038
Supporting Variants
SamplesNA20790
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6441610
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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