A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009844



Internal ID21919187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153450135..153454978hg38UCSC Ensembl
chr5:152829695..152834538hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg384844
hg194844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009844
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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