A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599010



Internal ID6986058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187319038..187321789hg38UCSC Ensembl
Innerchr3:187319051..187321777hg38UCSC Ensembl
Outerchr3:187319026..187321802hg38UCSC Ensembl
chr3:187036826..187039577hg19UCSC Ensembl
Innerchr3:187036839..187039565hg19UCSC Ensembl
Outerchr3:187036814..187039590hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382752
hg192752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11261126
SamplesHG01598
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599010
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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