A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395747



Internal ID21053300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133253229..133258189hg38UCSC Ensembl
chr5:132588921..132593881hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384961
hg194961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127171
Samples
Known GenesFSTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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