A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950259



Internal ID22725665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170407727..170407727hg38UCSC Ensembl
chr6:170716815..170716815hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950259
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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