A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11195384



Internal ID2851373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157884539..157899920hg38UCSC Ensembl
Innerchr3:157884539..157899920hg38UCSC Ensembl
Outerchr3:157884039..157900420hg38UCSC Ensembl
chr3:157602328..157617709hg19UCSC Ensembl
Innerchr3:157602328..157617709hg19UCSC Ensembl
Outerchr3:157601828..157618209hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3815382
hg1915382
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598323
Supporting Variants
SamplesHG02513
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11195384
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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