A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259449



Internal ID22064059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44702257..44702257hg38UCSC Ensembl
chrX:44561503..44561503hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17849206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259449
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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