A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133674



Internal ID20700714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58513593..58513831hg38UCSC Ensembl
chr5:57809420..57809658hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00123


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