A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136263



Internal ID20703303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99009413..99011778hg38UCSC Ensembl
chr5:98345117..98347482hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.7115


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