A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214131



Internal ID20781171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44686688..44719243hg38UCSC Ensembl
chr5:44686790..44719345hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3832556
hg1932556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214131
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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