A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102535



Internal ID22011768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5098595..5098595hg38UCSC Ensembl
chr21:45583208..45583208hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102535
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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