A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10938915



Internal ID4943717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16646733..16655580hg38UCSC Ensembl
Innerchr3:16646733..16655580hg38UCSC Ensembl
Outerchr3:16646233..16656080hg38UCSC Ensembl
chr3:16688240..16697087hg19UCSC Ensembl
Innerchr3:16688240..16697087hg19UCSC Ensembl
Outerchr3:16687740..16697587hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388848
hg198848
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595406
Supporting Variants
SamplesNA12813
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10938915
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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