A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717295



Internal ID140961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35234158..35343147hg38UCSC Ensembl
chr18:32814122..32923111hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38108990
hg19108990
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562609
Supporting Variants
Samples
Known GenesZNF24, ZNF271, ZNF397, ZSCAN30
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717295
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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