A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959735



Internal ID22734757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17171601..17171601hg38UCSC Ensembl
chr5:17171710..17171710hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424919
Samples
Known GenesLOC285696
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959735
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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