A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5750062



Internal ID8797127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17377985..17380991hg38UCSC Ensembl
Outerchr6:17377614..17381361hg38UCSC Ensembl
Innerchr6:17378216..17381222hg19UCSC Ensembl
Outerchr6:17377845..17381592hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383748
hg193748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666977
Supporting Variants
SamplesHG00243
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5750062
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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