A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102566



Internal ID22011799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79146464..79146464hg38UCSC Ensembl
chr18:76906464..76906464hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628035
Samples
Known GenesATP9B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102566
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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