A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001542



Internal ID20568582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55016176..55054025hg38UCSC Ensembl
chr12:55409960..55447809hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3837850
hg1937850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475074
Supporting Variants
Samples
Known GenesNEUROD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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