A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259750



Internal ID22064360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121169958..121169958hg38UCSC Ensembl
chrX:120303812..120303812hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259750
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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