A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556834



Internal ID329959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23310120..23985140hg38UCSC Ensembl
chr19:23492922..24167942hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38675021
hg19675021
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722528
Samples
Known GenesRPSAP58, ZNF675, ZNF681, ZNF726, ZNF91
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556834
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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