A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611718



Internal ID21803765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90789900..90800541hg38UCSC Ensembl
chr14:91256244..91266885hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3810642
hg1910642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035738
Supporting Variants
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611718
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