A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041432



Internal ID21950767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101096441..101096441hg38UCSC Ensembl
chr1:101561997..101561997hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041432
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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