A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407256



Internal ID21064809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108212084..108213925hg38UCSC Ensembl
chr5:107547785..107549626hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg381842
hg191842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122377
Samples
Known GenesFBXL17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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