A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956365



Internal ID22731556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41802435..41802435hg38UCSC Ensembl
chr6:41770173..41770173hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447565
Samples
Known GenesUSP49
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956365
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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