A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038794



Internal ID93608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96347735..96350933hg38UCSC Ensembl
chr10:98107492..98110690hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg383199
hg193199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474698
Supporting Variants
Samples
Known GenesOPALIN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038794
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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