A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016409



Internal ID21925752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175871399..175871458hg38UCSC Ensembl
chr5:175298402..175298461hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571680
Samples
Known GenesCPLX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016409
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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