A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031361



Internal ID20598401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67503134..67509484hg38UCSC Ensembl
chr16:67537037..67543387hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386351
hg196351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031361
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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