A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598981



Internal ID6986029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185935812..185939132hg38UCSC Ensembl
Innerchr3:185935812..185939132hg38UCSC Ensembl
Outerchr3:185935312..185939632hg38UCSC Ensembl
chr3:185653600..185656920hg19UCSC Ensembl
Innerchr3:185653600..185656920hg19UCSC Ensembl
Outerchr3:185653100..185657420hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg383321
hg193321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11257981, essv11257985, essv11257988, essv11257986, essv11257987, essv11257980, essv11257984, essv11257983, essv11257982
SamplesNA19443, NA18962, NA19307, NA19451, HG02511, NA19118, NA19031, NA19117, NA19312
Known GenesTRA2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598981
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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