A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190013



Internal ID20757053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75013433..75051604hg38UCSC Ensembl
chr16:75047331..75085502hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3838172
hg1938172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498518
Supporting Variants
Samples
Known GenesZNRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190013
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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