A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6085357



Internal ID9906029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29613663..29615128hg38UCSC Ensembl
chr8:29471179..29472644hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381466
hg191466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659359
Supporting Variants
SamplesNA20801
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6085357
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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