A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271564



Internal ID20480782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115633656..115634132hg38UCSC Ensembl
chr5:114969353..114969829hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271564
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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