A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137327



Internal ID20704367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122021122..122021688hg38UCSC Ensembl
chr6:122342268..122342834hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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