A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557024



Internal ID21881379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119558311..119558413hg38UCSC Ensembl
chr5:118894006..118894108hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016540
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557024
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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