A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6427019



Internal ID9404422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19197748..19198020hg38UCSC Ensembl
chr8:19055258..19055530hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664164
Supporting Variants
SamplesNA11918
Known GenesLOC100128993
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6427019
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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