A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596170



Internal ID6983487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53427584..53467104hg38UCSC Ensembl
Innerchr3:53427621..53467067hg38UCSC Ensembl
Outerchr3:53427547..53467141hg38UCSC Ensembl
chr3:53461611..53501131hg19UCSC Ensembl
Innerchr3:53461648..53501094hg19UCSC Ensembl
Outerchr3:53461574..53501168hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3839521
hg1939521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11014142
SamplesHG04107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596170
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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