A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14899364



Internal ID980154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112175183..112182939hg38UCSC Ensembl
chr13:112829497..112837253hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg387757
hg197757
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633574
Supporting Variants
SamplesHG00610
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14899364
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