A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134277



Internal ID20701317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89897544..89898212hg38UCSC Ensembl
chr5:89193361..89194029hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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