A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180472



Internal ID20747512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77723713..77724236hg38UCSC Ensembl
chr16:77757610..77758133hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513460
Supporting Variants
Samples
Known GenesNUDT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180472
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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