A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119644



Internal ID20686684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8455149..8457461hg38UCSC Ensembl
chr4:8456876..8459188hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg382313
hg192313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357996
Supporting Variants
Samples
Known GenesTRMT44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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