A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956254



Internal ID22731446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132037769..132037769hg38UCSC Ensembl
chrX:131171797..131171797hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441581
Samples
Known GenesMST4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956254
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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