A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5620708



Internal ID8598111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93785902..93786215hg38UCSC Ensembl
chr1:94251458..94251771hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660297
Supporting Variants
SamplesNA18964
Known GenesBCAR3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5620708
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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