A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068325



Internal ID21977558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23624246..23624246hg38UCSC Ensembl
chr6:23624474..23624474hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068325
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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