A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701136



Internal ID124802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41561310..41570238hg38UCSC Ensembl
chr15:41853508..41862436hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg388929
hg198929
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556172
Supporting Variants
Samples
Known GenesTYRO3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701136
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.110677


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