A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550811



Internal ID21875166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7262340..7268946hg38UCSC Ensembl
chr5:7262453..7269059hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg386607
hg196607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000276
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550811
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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