A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618015



Internal ID6658210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91174627..91176814hg38UCSC Ensembl
Innerchr8:91174634..91176808hg38UCSC Ensembl
Outerchr8:91174621..91176821hg38UCSC Ensembl
chr8:92186855..92189042hg19UCSC Ensembl
Innerchr8:92186862..92189036hg19UCSC Ensembl
Outerchr8:92186849..92189049hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg382188
hg192188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13254106, essv13254107
SamplesNA19375, HG02807
Known GenesLRRC69
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618015
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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