A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025597



Internal ID21934940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23204298..23204360hg38UCSC Ensembl
chr16:23215619..23215681hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605471
Samples
Known GenesSCNN1G
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025597
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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