A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214984



Internal ID20782024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88590642..88614616hg38UCSC Ensembl
chr5:87886460..87910434hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3823975
hg1923975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398388
Supporting Variants
Samples
Known GenesLINC00461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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