A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031812



Internal ID88926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25718869..25772034hg38UCSC Ensembl
chr10:26007798..26060963hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3853166
hg1953166
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554728
Supporting Variants
Samples
Known GenesLINC00836
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031812
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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