A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105661



Internal ID22014894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76975159..76975159hg38UCSC Ensembl
chr18:74687115..74687115hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105661
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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