A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5511607



Internal ID8928459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10218274..10236640hg38UCSC Ensembl
Outerchr8:10218237..10236690hg38UCSC Ensembl
Innerchr8:10075784..10094150hg19UCSC Ensembl
Outerchr8:10075747..10094200hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3818454
hg1918454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659013
Supporting Variants
SamplesHG00437
Known GenesMSRA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5511607
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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