A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598121



Internal ID6985257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147821203..147886223hg38UCSC Ensembl
Innerchr3:147821203..147886223hg38UCSC Ensembl
Outerchr3:147820703..147886723hg38UCSC Ensembl
chr3:147538990..147604010hg19UCSC Ensembl
Innerchr3:147538990..147604010hg19UCSC Ensembl
Outerchr3:147538490..147604510hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3865021
hg1965021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11176532
SamplesNA19731
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598121
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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