A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133381



Internal ID20700421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78749691..78756487hg38UCSC Ensembl
chr5:78045514..78052310hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg386797
hg196797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414322
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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