A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661524



Internal ID9927629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88747268..88747531hg38UCSC Ensembl
chr8:89759497..89759760hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6525950, essv5775597, essv5722065, essv6286254, essv6589480, essv5820864
SamplesNA19703, NA19397, HG01462, NA19914, NA19396, NA19398
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661524
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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