A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717672



Internal ID141338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42151366..42213909hg38UCSC Ensembl
chr18:39731330..39793874hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3862544
hg1962545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532079
Supporting Variants
Samples
Known GenesLINC00907
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717672
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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