A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038766



Internal ID93589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95864189..95864271hg38UCSC Ensembl
chr10:97623946..97624028hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473973
Supporting Variants
Samples
Known GenesENTPD1, ENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038766
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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