A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598860



Internal ID6972378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180132497..180145454hg38UCSC Ensembl
Innerchr3:180132497..180145454hg38UCSC Ensembl
Outerchr3:180131997..180145954hg38UCSC Ensembl
chr3:179850285..179863242hg19UCSC Ensembl
Innerchr3:179850285..179863242hg19UCSC Ensembl
Outerchr3:179849785..179863742hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3812958
hg1912958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11248433
SamplesHG03753
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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