A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967822



Internal ID22742757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47796754..47796754hg38UCSC Ensembl
chr15:48088951..48088951hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967822
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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