A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213425



Internal ID20780465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37155057..37598230hg38UCSC Ensembl
chr5:37155159..37598332hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38443174
hg19443174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381631
Supporting Variants
Samples
Known GenesC5orf42, NUP155, WDR70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213425
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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