A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135776



Internal ID20702816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10054501..10056800hg38UCSC Ensembl
chr6:10054734..10057033hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135776
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