A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6243100



Internal ID22047710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21212065..21212065hg38UCSC Ensembl
chrY:23373951..23373951hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6243100
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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