A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507992



Internal ID20881289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23328402..23346794hg38UCSC Ensembl
chr16:23339723..23358115hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3818393
hg1918393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028792
Samples
Known GenesSCNN1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507992
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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