A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618016



Internal ID6658211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91174869..91178530hg38UCSC Ensembl
Innerchr8:91174869..91178530hg38UCSC Ensembl
Outerchr8:91174706..91178709hg38UCSC Ensembl
chr8:92187097..92190758hg19UCSC Ensembl
Innerchr8:92187097..92190758hg19UCSC Ensembl
Outerchr8:92186934..92190937hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg383662
hg193662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13254108, essv13254109
SamplesNA19375, HG02807
Known GenesLRRC69
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618016
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer