A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242953



Internal ID22047563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129112270..129112270hg38UCSC Ensembl
chrX:128246247..128246247hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850117
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242953
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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