A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090636



Internal ID21999869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:858247..858247hg38UCSC Ensembl
chr16:908247..908247hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607164
Samples
Known GenesLMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090636
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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