A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11236071



Internal ID528774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176476932..176480156hg38UCSC Ensembl
Innerchr3:176476945..176480143hg38UCSC Ensembl
Outerchr3:176476919..176480169hg38UCSC Ensembl
chr3:176194720..176197944hg19UCSC Ensembl
Innerchr3:176194733..176197931hg19UCSC Ensembl
Outerchr3:176194707..176197957hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383225
hg193225
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598768
Supporting Variants
SamplesHG00190
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11236071
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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