A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6171077



Internal ID8919552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:34697057..34698942hg38UCSC Ensembl
Outerchr8:34696900..34699095hg38UCSC Ensembl
Innerchr8:34554575..34556460hg19UCSC Ensembl
Outerchr8:34554418..34556613hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382196
hg192196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663372
Supporting Variants
SamplesHG00421
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6171077
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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