A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608409



Internal ID21800456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99577804..99578176hg38UCSC Ensembl
chr14:100044141..100044513hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034544
Supporting Variants
Samples
Known GenesCCDC85C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608409
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