A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016378



Internal ID21925721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94625454..94625543hg38UCSC Ensembl
chr5:93961159..93961248hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557192
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016378
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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