A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925380



Internal ID22700607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166481622..166482117hg38UCSC Ensembl
chr6:166895110..166895605hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410550
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925380
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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