A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038767



Internal ID93590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95895564..95895630hg38UCSC Ensembl
chr10:97655321..97655387hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479469
Supporting Variants
Samples
Known GenesENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038767
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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