A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036033



Internal ID20603073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40479426..40481561hg38UCSC Ensembl
chr17:38635678..38637813hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382136
hg192136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500298
Supporting Variants
Samples
Known GenesTNS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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