A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267455



Internal ID20476673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87302618..87302618hg38UCSC Ensembl
chr5:86598435..86598435hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754072
Supporting Variants
Samples
Known GenesRASA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267455
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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