A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11164652



Internal ID4006939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142584970..142591972hg38UCSC Ensembl
Innerchr3:142584978..142591964hg38UCSC Ensembl
Outerchr3:142584962..142591980hg38UCSC Ensembl
chr3:142303812..142310814hg19UCSC Ensembl
Innerchr3:142303820..142310806hg19UCSC Ensembl
Outerchr3:142303804..142310822hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg387003
hg197003
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598005
Supporting Variants
SamplesHG03660
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11164652
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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