A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900188



Internal ID915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25217675..25219153hg38UCSC Ensembl
chr1:25544166..25545644hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900188
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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