A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005457



Internal ID21914800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9523560..9535485hg38UCSC Ensembl
chr6:9523793..9535718hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3811926
hg1911926
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005457
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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