A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612615



Internal ID21804662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23208595..23208683hg38UCSC Ensembl
chr16:23219916..23220004hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035242
Supporting Variants
Samples
Known GenesSCNN1G
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612615
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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