A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061901



Internal ID21971134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27845212..27845212hg38UCSC Ensembl
chr6:27812990..27812990hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg382775
hg192775
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061901
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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