A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268768



Internal ID20477986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132275299..132275359hg38UCSC Ensembl
chr5:131610992..131611052hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736940
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268768
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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