A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145863



Internal ID20712903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55918712..55919344hg38UCSC Ensembl
chr6:55783510..55784142hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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