A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213274



Internal ID20780314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149302970..149309698hg38UCSC Ensembl
chr5:148682533..148689261hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386729
hg196729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405777
Supporting Variants
Samples
Known GenesAFAP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213274
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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