A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117295



Internal ID20684335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5170635..5343284hg38UCSC Ensembl
chr4:5172362..5345011hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38172650
hg19172650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374355
Supporting Variants
Samples
Known GenesSTK32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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