A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6054936



Internal ID9892249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:59930772..59955877hg38UCSC Ensembl
Outerchr8:59930735..59955927hg38UCSC Ensembl
Innerchr8:60843331..60868436hg19UCSC Ensembl
Outerchr8:60843294..60868486hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3825193
hg1925193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659572
Supporting Variants
SamplesNA20772
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6054936
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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