A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122344



Internal ID20689384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107939699..107945143hg38UCSC Ensembl
chr5:107275400..107280844hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg385445
hg195445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397221
Supporting Variants
Samples
Known GenesFBXL17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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