A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6195224



Internal ID9172627
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
SamplesNA12892
Known GenesLOC100128993
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6195224
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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