A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117430



Internal ID20684470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53791420..53792641hg38UCSC Ensembl
chr4:54657587..54658808hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117430
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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