A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292619



Internal ID20501837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173699670..173699860hg38UCSC Ensembl
chr5:173126673..173126863hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742704
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292619
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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