A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178714



Internal ID20745754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9151884..9245875hg38UCSC Ensembl
chr16:9245741..9339732hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3893992
hg1993992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512048
Supporting Variants
Samples
Known GenesMIR548X
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178714
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