A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276663



Internal ID20485881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111531936..111531994hg38UCSC Ensembl
chr5:110867634..110867692hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737346
Supporting Variants
Samples
Known GenesSTARD4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276663
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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