A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213225



Internal ID20780265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142646163..142646766hg38UCSC Ensembl
chr5:142025728..142026331hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410550
Supporting Variants
Samples
Known GenesFGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213225
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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