A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11266336



Internal ID4150223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189404430..189427189hg38UCSC Ensembl
Innerchr3:189404461..189427159hg38UCSC Ensembl
Outerchr3:189404400..189427220hg38UCSC Ensembl
chr3:189122219..189144978hg19UCSC Ensembl
Innerchr3:189122250..189144948hg19UCSC Ensembl
Outerchr3:189122189..189145009hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3822760
hg1922760
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599054
Supporting Variants
SamplesHG03755
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11266336
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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