A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031301



Internal ID20598341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66691172..66695683hg38UCSC Ensembl
chr16:66725075..66729586hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg384512
hg194512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510480
Supporting Variants
Samples
Known GenesCMTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031301
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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