A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135994



Internal ID20703035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86284604..86286138hg38UCSC Ensembl
chr5:85580422..85581956hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381535
hg191535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398989
Supporting Variants
Samples
Known GenesNBPF22P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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