A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022511



Internal ID20589551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97663688..97674612hg38UCSC Ensembl
chr14:98130025..98140949hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810925
hg1910925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508867
Supporting Variants
Samples
Known GenesLOC100129345
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0027


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