A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571724



Internal ID21763767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168513683..168513683hg38UCSC Ensembl
chr5:167940688..167940688hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075394
Supporting Variants
Samples
Known GenesRARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571724
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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