A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007382



Internal ID21916725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154525802..154528303hg38UCSC Ensembl
chr6:154846936..154849437hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007382
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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