A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715951



Internal ID139617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3765969..3770697hg38UCSC Ensembl
chr18:3765969..3770697hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg384729
hg194729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525246
Supporting Variants
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715951
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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