A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038276



Internal ID93244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85614563..85614636hg38UCSC Ensembl
chr10:87374320..87374393hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486248
Supporting Variants
Samples
Known GenesGRID1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038276
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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