A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001202



Internal ID21910545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170607038..170743761hg38UCSC Ensembl
chr6:170916126..171052849hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38136724
hg19136724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001202
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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