A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595784



Internal ID6983102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32824713..32828913hg38UCSC Ensembl
Innerchr3:32824763..32828863hg38UCSC Ensembl
Outerchr3:32824663..32828963hg38UCSC Ensembl
chr3:32866205..32870405hg19UCSC Ensembl
Innerchr3:32866255..32870355hg19UCSC Ensembl
Outerchr3:32866155..32870455hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg384201
hg194201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10977916
SamplesHG03304
Known GenesTRIM71
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595784
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