A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998255



Internal ID20565295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22187972..22188700hg38UCSC Ensembl
chr12:22340906..22341634hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467128
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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