A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051541



Internal ID21960774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55480383..55480383hg38UCSC Ensembl
chr2:55707519..55707519hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051541
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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