A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124149



Internal ID20691189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106885858..106925319hg38UCSC Ensembl
chr5:106221559..106261020hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3839462
hg1939462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409281
Supporting Variants
Samples
Known GenesLOC102467213
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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