A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397590



Internal ID21055143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54369201..54384100hg38UCSC Ensembl
chr5:53665031..53679930hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3814900
hg1914900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397590
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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