A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546609



Internal ID21870964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87302622..87302622hg38UCSC Ensembl
chr5:86598439..86598439hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072966
Supporting Variants
Samples
Known GenesRASA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546609
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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