A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716385



Internal ID140051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13673070..13673764hg38UCSC Ensembl
chr18:13673069..13673763hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530510
Supporting Variants
Samples
Known GenesFAM210A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716385
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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