A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036869



Internal ID92334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91055641..91055947hg38UCSC Ensembl
chr10:92815398..92815704hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485140
Supporting Variants
Samples
Known GenesLINC00502
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036869
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.158133


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