A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087611



Internal ID21996844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50563960..50563960hg38UCSC Ensembl
chr16:50597871..50597871hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623112
Samples
Known GenesNKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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