A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129544



Internal ID20696584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168847504..168849105hg38UCSC Ensembl
chr5:168274509..168276110hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401346
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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