A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607176



Internal ID21799223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130022223..130022276hg38UCSC Ensembl
chr11:129892118..129892171hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607176
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