A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595964



Internal ID6983282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41048352..41103595hg38UCSC Ensembl
Innerchr3:41048354..41103594hg38UCSC Ensembl
Outerchr3:41048351..41103597hg38UCSC Ensembl
chr3:41089843..41145086hg19UCSC Ensembl
Innerchr3:41089845..41145085hg19UCSC Ensembl
Outerchr3:41089842..41145088hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3855244
hg1955244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10989678
SamplesHG03900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595964
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