A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956624



Internal ID22731800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16690216..16690216hg38UCSC Ensembl
chrX:16708339..16708339hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447518
Samples
Known GenesCTPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956624
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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