A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900231



Internal ID946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25573854..25581550hg38UCSC Ensembl
chr1:25900345..25908041hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387697
hg197697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900231
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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