A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598085



Internal ID6985221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146039295..146043059hg38UCSC Ensembl
Innerchr3:146039320..146043034hg38UCSC Ensembl
Outerchr3:146039270..146043084hg38UCSC Ensembl
chr3:145757082..145760846hg19UCSC Ensembl
Innerchr3:145757107..145760821hg19UCSC Ensembl
Outerchr3:145757057..145760871hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg383765
hg193765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11172886
SamplesNA19017
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598085
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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