A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959227



Internal ID22734266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9861037..9861037hg38UCSC Ensembl
chr5:9861149..9861149hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410301
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959227
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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