A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035242



Internal ID21944585
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 StatusM
Merged Variants
Supporting Variantsnssv17612615
Samples
Known GenesSCNN1G
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035242
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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