A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134929



Internal ID20701969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90518694..90519509hg38UCSC Ensembl
chr5:89814511..89815326hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405379
Supporting Variants
Samples
Known GenesLYSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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