A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6243059



Internal ID22047669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154849478..154849478hg38UCSC Ensembl
chrX:154077753..154077753hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851715
Samples
Known GenesF8
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6243059
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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