A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538557



Internal ID21862912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17611562..17823922hg38UCSC Ensembl
chr5:17611671..17824031hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38212361
hg19212361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999056
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538557
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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