A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562609



Internal ID335557
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 StatusM
Merged Variants
Supporting Variantsnssv17717295
Samples
Known GenesZNF24, ZNF271, ZNF397, ZSCAN30
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562609
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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