A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598845



Internal ID6639110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179626415..179627290hg38UCSC Ensembl
Innerchr3:179626438..179627267hg38UCSC Ensembl
Outerchr3:179626392..179627313hg38UCSC Ensembl
chr3:179344203..179345078hg19UCSC Ensembl
Innerchr3:179344226..179345055hg19UCSC Ensembl
Outerchr3:179344180..179345101hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38876
hg19876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11244533, essv11244534
SamplesNA19443, HG03095
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598845
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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