A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016631



Internal ID21925974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96328365..96328419hg38UCSC Ensembl
chr5:95664069..95664123hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016631
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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