A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048544



Internal ID21957777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16164054..16164054hg38UCSC Ensembl
chr1:16490549..16490549hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048544
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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