A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11036146



Internal ID6929170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69159620..69161835hg38UCSC Ensembl
Innerchr3:69159670..69161785hg38UCSC Ensembl
Outerchr3:69159570..69161885hg38UCSC Ensembl
chr3:69208771..69210986hg19UCSC Ensembl
Innerchr3:69208821..69210936hg19UCSC Ensembl
Outerchr3:69208721..69211036hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382216
hg192216
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596494
Supporting Variants
SamplesNA21122
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11036146
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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