A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549199



Internal ID21873554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43983061..43989955hg38UCSC Ensembl
chr5:43983163..43990057hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg386895
hg196895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999697
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549199
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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