A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596657



Internal ID6636927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77225621..77227784hg38UCSC Ensembl
Innerchr3:77225646..77227760hg38UCSC Ensembl
Outerchr3:77225597..77227809hg38UCSC Ensembl
chr3:77274772..77276935hg19UCSC Ensembl
Innerchr3:77274797..77276911hg19UCSC Ensembl
Outerchr3:77274748..77276960hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg382164
hg192164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11048847, essv11048848, essv11048849
SamplesHG03965, HG03790, HG03814
Known GenesROBO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596657
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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