A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002388



Internal ID21911731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73563270..73563841hg38UCSC Ensembl
chr6:74272993..74273564hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002388
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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