A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117562



Internal ID20684602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44687878..44688390hg38UCSC Ensembl
chr4:44689895..44690407hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378812
Supporting Variants
Samples
Known GenesGUF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117562
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00079


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