A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002709



Internal ID21912052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123941586..123948568hg38UCSC Ensembl
chr5:123277280..123284262hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg386983
hg196983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002709
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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