A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031273



Internal ID20598313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66443865..66453923hg38UCSC Ensembl
chr16:66477768..66487826hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3810059
hg1910059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501341
Supporting Variants
Samples
Known GenesBEAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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