A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003671



Internal ID21913014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146520229..146522723hg38UCSC Ensembl
chr5:145899792..145902286hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382495
hg192495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003671
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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