A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029924



Internal ID20596964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48571501..48574919hg38UCSC Ensembl
chr16:48605412..48608830hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383419
hg193419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501388
Supporting Variants
Samples
Known GenesN4BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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