A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424919



Internal ID22482789
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 StatusS
Merged Variantsnsv5959735
Supporting Variants
Samples
Known GenesLOC285696
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424919
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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