A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087728



Internal ID21996961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24316244..24316244hg38UCSC Ensembl
chr16:24327565..24327565hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609102
Samples
Known GenesCACNG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087728
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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