A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595938



Internal ID6983256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39858759..39859231hg38UCSC Ensembl
Innerchr3:39858789..39859202hg38UCSC Ensembl
Outerchr3:39858730..39859261hg38UCSC Ensembl
chr3:39900250..39900722hg19UCSC Ensembl
Innerchr3:39900280..39900693hg19UCSC Ensembl
Outerchr3:39900221..39900752hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10987886
SamplesNA18544
Known GenesMYRIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595938
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer