A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034616



Internal ID20601656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16427416..16429470hg38UCSC Ensembl
chr17:16330730..16332784hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382055
hg192055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504677
Supporting Variants
Samples
Known GenesTRPV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034616
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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