A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553406



Internal ID21877761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135784785..135784785hg38UCSC Ensembl
chr5:135120474..135120474hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073670
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553406
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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