A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014606



Internal ID21923949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167997398..167997522hg38UCSC Ensembl
chr6:168398078..168398202hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014606
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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