A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414983



Internal ID21072536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157950483..157964644hg38UCSC Ensembl
chr5:157377491..157391652hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3814162
hg1914162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215916
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414983
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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