A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003869



Internal ID21913212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139442442..139447839hg38UCSC Ensembl
chr5:138778131..138783528hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg385398
hg195398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003869
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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