A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555146



Internal ID328312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61122738..61127611hg38UCSC Ensembl
chr18:58789971..58794844hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg384874
hg194874
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17718690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555146
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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