A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396896



Internal ID21054449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133388195..133407711hg38UCSC Ensembl
chr5:132723887..132743403hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3819517
hg1919517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215873
Samples
Known GenesFSTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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