A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900430



Internal ID1070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27203522..27209966hg38UCSC Ensembl
chr1:27530013..27536457hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386445
hg196445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416160
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900430
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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