A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11222028



Internal ID1223844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169717756..169735690hg38UCSC Ensembl
Innerchr3:169718256..169735190hg38UCSC Ensembl
Outerchr3:169716756..169736690hg38UCSC Ensembl
chr3:169435544..169453478hg19UCSC Ensembl
Innerchr3:169436044..169452978hg19UCSC Ensembl
Outerchr3:169434544..169454478hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3817935
hg1917935
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598602
Supporting Variants
SamplesHG03085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11222028
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