A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125722



Internal ID20692762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117000961..117004545hg38UCSC Ensembl
chr5:116336657..116340241hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg383585
hg193585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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