A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471173



Internal ID22529064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31155093..31159037hg38UCSC Ensembl
chr15:31447296..31451240hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383945
hg193945
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852031
Supporting Variants
Samples
Known GenesTRPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471173
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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