A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100889



Internal ID22010122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2614547..2614547hg38UCSC Ensembl
chr18:2614546..2614546hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622676
Samples
Known GenesNDC80
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100889
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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