A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715445



Internal ID139111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11610000..11645000hg38UCSC Ensembl
chr18:11609999..11644999hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3835001
hg1935001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532173
Supporting Variants
Samples
Known GenesSLC35G4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715445
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007049


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