A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141431



Internal ID20708471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30281678..30287536hg38UCSC Ensembl
chr6:30249455..30255313hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg385859
hg195859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411255
Supporting Variants
Samples
Known GenesHCG17, HCG18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141431
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