A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031781



Internal ID20598821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69342155..69347522hg38UCSC Ensembl
chr16:69376058..69381425hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg385368
hg195368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507793
Supporting Variants
Samples
Known GenesNIP7, TMED6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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