A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553764



Internal ID21878119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:898458..898901hg38UCSC Ensembl
chr5:898573..899016hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000289
Supporting Variants
Samples
Known GenesTRIP13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553764
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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