A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616971



Internal ID21809018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74886019..74886019hg38UCSC Ensembl
chr14:75352722..75352722hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087068
Supporting Variants
Samples
Known GenesDLST
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616971
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer