A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289210



Internal ID20498428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68810103..68810197hg38UCSC Ensembl
chr5:68105930..68106024hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749002
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289210
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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