A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624516



Internal ID21816563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36192747..36192823hg38UCSC Ensembl
chr18:33772710..33772786hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037750
Supporting Variants
Samples
Known GenesMOCOS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624516
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