A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096044



Internal ID22005277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23204314..23204314hg38UCSC Ensembl
chr16:23215635..23215635hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607467
Samples
Known GenesSCNN1G
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096044
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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