A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924851



Internal ID22700078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166783873..166784545hg38UCSC Ensembl
chr6:167197361..167198033hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428950
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924851
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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