A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595097



Internal ID6982416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4195279..4246093hg38UCSC Ensembl
Innerchr3:4195322..4246050hg38UCSC Ensembl
Outerchr3:4195236..4246136hg38UCSC Ensembl
chr3:4236963..4287777hg19UCSC Ensembl
Innerchr3:4237006..4287734hg19UCSC Ensembl
Outerchr3:4236920..4287820hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3850815
hg1950815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10905322, essv10905319, essv10905325, essv10905328, essv10905323, essv10905320, essv10905324, essv10905326, essv10905321, essv10905329, essv10905327
SamplesNA18745, HG03193, NA18988, NA18635, NA18557, HG02221, NA18548, NA18533, NA19779, HG03313, NA11892
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595097
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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