A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050835



Internal ID20617875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109941502..109943177hg38UCSC Ensembl
chr1:110484124..110485799hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00087


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