A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597232



Internal ID6972166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103731073..103759572hg38UCSC Ensembl
Innerchr3:103731073..103759572hg38UCSC Ensembl
Outerchr3:103730573..103760072hg38UCSC Ensembl
chr3:103449917..103478416hg19UCSC Ensembl
Innerchr3:103449917..103478416hg19UCSC Ensembl
Outerchr3:103449417..103478916hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3828500
hg1928500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11090427
SamplesHG01923
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597232
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