A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508298



Internal ID20881597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23294814..23308830hg38UCSC Ensembl
chr16:23306135..23320151hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3814017
hg1914017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028791
Samples
Known GenesSCNN1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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