A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636351



Internal ID21828398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3599450..3599450hg38UCSC Ensembl
chr17:3502744..3502744hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099874
Supporting Variants
Samples
Known GenesTRPV1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636351
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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