A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11194908



Internal ID5570946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157065487..157067175hg38UCSC Ensembl
Innerchr3:157065509..157067153hg38UCSC Ensembl
Outerchr3:157065465..157067197hg38UCSC Ensembl
chr3:156783276..156784964hg19UCSC Ensembl
Innerchr3:156783298..156784942hg19UCSC Ensembl
Outerchr3:156783254..156784986hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381689
hg191689
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598309
Supporting Variants
SamplesNA19019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11194908
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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