A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898554



Internal ID22673671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159797716..159797956hg38UCSC Ensembl
chr6:160218748..160218988hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413163
Samples
Known GenesMRPL18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898554
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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