A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546978



Internal ID21871333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69361447..69361447hg38UCSC Ensembl
chr5:68657274..68657274hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063193
Supporting Variants
Samples
Known GenesAK6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546978
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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