A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543903



Internal ID21868258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113341292..113346405hg38UCSC Ensembl
chr5:112676989..112682102hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg385114
hg195114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008429
Supporting Variants
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543903
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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