A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414713



Internal ID21072266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108052494..108058929hg38UCSC Ensembl
chr5:107388195..107394630hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg386436
hg196436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122361
Samples
Known GenesFBXL17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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