A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051308



Internal ID21960541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152471415..152471415hg38UCSC Ensembl
chr1:152443891..152443891hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg385961
hg195961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051308
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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