A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954129



Internal ID22729389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158803561..158803561hg38UCSC Ensembl
chr6:159224593..159224593hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417592
Samples
Known GenesEZR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954129
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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