A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213271



Internal ID20780311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14818618..14845127hg38UCSC Ensembl
chr5:14818727..14845236hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3826510
hg1926510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376879
Supporting Variants
Samples
Known GenesANKH, MIR4637
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213271
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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