A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048052



Internal ID21957285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182065183..182065183hg38UCSC Ensembl
chr1:182034318..182034318hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048052
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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