A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547154



Internal ID21871509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135452392..135452454hg38UCSC Ensembl
chr5:134788082..134788144hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003365
Supporting Variants
Samples
Known GenesTIFAB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547154
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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