A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6250562



Internal ID22055172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3599491..3599491hg38UCSC Ensembl
chr17:3502785..3502785hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848047
Samples
Known GenesTRPV1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6250562
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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