A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557727



Internal ID330816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76996682..76997928hg38UCSC Ensembl
chr18:74708638..74709884hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719671
Samples
Known GenesMBP
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557727
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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