A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596057



Internal ID6636331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46026011..46027401hg38UCSC Ensembl
Innerchr3:46026011..46027401hg38UCSC Ensembl
Outerchr3:46025739..46027631hg38UCSC Ensembl
chr3:46067503..46068893hg19UCSC Ensembl
Innerchr3:46067503..46068893hg19UCSC Ensembl
Outerchr3:46067231..46069123hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10998876, essv10998875
SamplesHG02554, HG02979
Known GenesXCR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596057
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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