A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950451



Internal ID22725851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61033161..61033161hg38UCSC Ensembl
chr8:61945720..61945720hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950451
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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