A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423478



Internal ID22481348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17287321..17289164hg38UCSC Ensembl
chr6:17287552..17289395hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898619
Supporting Variants
Samples
Known GenesRBM24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423478
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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