A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548212



Internal ID21872567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56038872..56039008hg38UCSC Ensembl
chr5:55334699..55334835hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999983
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548212
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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