A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580086



Internal ID21772129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32657100..32668151hg38UCSC Ensembl
chr11:32678646..32689697hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811052
hg1911052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036189
Supporting Variants
Samples
Known GenesCCDC73
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580086
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