A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043553



Internal ID21952847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101371176..101371176hg38UCSC Ensembl
chr1:101836732..101836732hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg382163
hg192163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043553
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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