A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11213107



Internal ID4315920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163606690..163644837hg38UCSC Ensembl
Innerchr3:163607190..163644337hg38UCSC Ensembl
Outerchr3:163605690..163645837hg38UCSC Ensembl
chr3:163324478..163362625hg19UCSC Ensembl
Innerchr3:163324978..163362125hg19UCSC Ensembl
Outerchr3:163323478..163363625hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3838148
hg1938148
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598463
Supporting Variants
SamplesHG03867
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11213107
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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