A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597300



Internal ID6972234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107113829..107115456hg38UCSC Ensembl
Innerchr3:107113831..107115455hg38UCSC Ensembl
Outerchr3:107113828..107115458hg38UCSC Ensembl
chr3:106832676..106834303hg19UCSC Ensembl
Innerchr3:106832678..106834302hg19UCSC Ensembl
Outerchr3:106832675..106834305hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg381628
hg191628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11094679
SamplesHG03079
Known GenesLINC00882
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597300
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