A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129256



Internal ID20696296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180255887..180258663hg38UCSC Ensembl
chr5:179682887..179685663hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382777
hg192777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408026
Supporting Variants
Samples
Known GenesMAPK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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