A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965875



Internal ID22740810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14899114..14899114hg38UCSC Ensembl
chrX:14917236..14917236hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435884
Samples
Known GenesMOSPD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965875
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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