A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630213



Internal ID21822260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3535254..3535254hg38UCSC Ensembl
chr17:3438548..3438548hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080832
Supporting Variants
Samples
Known GenesTRPV3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630213
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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