A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925954



Internal ID22701181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166585488..166586677hg38UCSC Ensembl
chr6:166998976..167000165hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427588
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925954
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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