A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595245



Internal ID6982563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9597568..9602152hg38UCSC Ensembl
Innerchr3:9597588..9602133hg38UCSC Ensembl
Outerchr3:9597549..9602172hg38UCSC Ensembl
chr3:9639252..9643836hg19UCSC Ensembl
Innerchr3:9639272..9643817hg19UCSC Ensembl
Outerchr3:9639233..9643856hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384585
hg194585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10917795, essv10917785, essv10917787, essv10917788, essv10917794, essv10917786, essv10917793, essv10917790, essv10917792, essv10917791, essv10917789
SamplesNA19141, NA19332, HG02811, NA19131, HG02502, NA19209, NA20318, HG03160, NA19175, HG02953, NA19019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595245
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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