A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605408



Internal ID21797455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124929697..124930024hg38UCSC Ensembl
chr11:124799593..124799920hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021596
Supporting Variants
Samples
Known GenesHEPACAM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605408
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