A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5894205



Internal ID8958905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101623426..101623658hg38UCSC Ensembl
chr8:102635654..102635886hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657338
Supporting Variants
SamplesHG00525
Known GenesGRHL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5894205
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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