A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265805



Internal ID20475023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2862397..2863001hg38UCSC Ensembl
chr5:2862511..2863115hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265805
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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