A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415718



Internal ID194968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56084943..56084994hg38UCSC Ensembl
chr18:53752174..53752225hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17718401
Samples
Known GenesLOC100505474
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415718
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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