A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287456



Internal ID20496674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168513681..168513681hg38UCSC Ensembl
chr5:167940686..167940686hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753594
Supporting Variants
Samples
Known GenesRARS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287456
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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