A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036698



Internal ID21946041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57502979..57506493hg38UCSC Ensembl
chr13:58077113..58080627hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg383515
hg193515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036698
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer