A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396034



Internal ID22453904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5691452..5691529hg38UCSC Ensembl
chr19:5691463..5691540hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939731
Supporting Variants
Samples
Known GenesRPL36
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396034
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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