A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021165



Internal ID21930508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23314697..23339044hg38UCSC Ensembl
chr16:23326018..23350365hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3824348
hg1924348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601875
Samples
Known GenesSCNN1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021165
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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