A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007216



Internal ID21916559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171623263..171623315hg38UCSC Ensembl
chr5:171050267..171050319hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007216
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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