A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268034



Internal ID20477252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181253132..181254470hg38UCSC Ensembl
chr5:180680132..180681470hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg381339
hg191339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268034
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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