A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030342



Internal ID20597382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51687282..51690311hg38UCSC Ensembl
chr16:51721193..51724222hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383030
hg193030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030342
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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