A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742333



Internal ID20518315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14899131..14899131hg38UCSC Ensembl
chrX:14917253..14917253hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260475
Samples
Known GenesMOSPD2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742333
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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