A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007132



Internal ID21916475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128058538..128058609hg38UCSC Ensembl
chr5:127394230..127394301hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553758
Samples
Known GenesFLJ33630
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007132
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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