A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214213



Internal ID20781253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80408015..80415588hg38UCSC Ensembl
chr5:79703834..79711407hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg387574
hg197574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414899
Supporting Variants
Samples
Known GenesZFYVE16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214213
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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