A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562819



Internal ID335760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32785582..32797853hg38UCSC Ensembl
chr18:30365545..30377816hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3812272
hg1912272
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562819
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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