A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181532



Internal ID20748572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96794401..96800500hg38UCSC Ensembl
chr14:97260738..97266837hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503502
Supporting Variants
Samples
Known GenesVRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181532
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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