A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110184



Internal ID22019417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76978883..76978883hg38UCSC Ensembl
chr18:74690839..74690839hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632605
Samples
Known GenesMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110184
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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