A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10939868



Internal ID4932805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18315208..18318365hg38UCSC Ensembl
Innerchr3:18315223..18318351hg38UCSC Ensembl
Outerchr3:18315194..18318380hg38UCSC Ensembl
chr3:18356700..18359857hg19UCSC Ensembl
Innerchr3:18356715..18359843hg19UCSC Ensembl
Outerchr3:18356686..18359872hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383158
hg193158
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595432
Supporting Variants
SamplesNA12776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10939868
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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