A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037401



Internal ID92686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68153146..68153146hg38UCSC Ensembl
chr10:69912903..69912903hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559297
Supporting Variants
Samples
Known GenesMYPN
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037401
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.005151


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