A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6243068



Internal ID22047678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3720057..3720057hg38UCSC Ensembl
chrY:3588098..3588098hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6243068
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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