A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213427



Internal ID20780467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37233015..37632885hg38UCSC Ensembl
chr5:37233117..37632987hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38399871
hg19399871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385721
Supporting Variants
Samples
Known GenesC5orf42, NUP155, WDR70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213427
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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