A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11238201



Internal ID854589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177935741..177938287hg38UCSC Ensembl
Innerchr3:177935757..177938271hg38UCSC Ensembl
Outerchr3:177935725..177938303hg38UCSC Ensembl
chr3:177653529..177656075hg19UCSC Ensembl
Innerchr3:177653545..177656059hg19UCSC Ensembl
Outerchr3:177653513..177656091hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382547
hg192547
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598809
Supporting Variants
SamplesHG00446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11238201
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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