A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972055



Internal ID22746990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:297709..309674hg38UCSC Ensembl
chrX:214376..226341hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3811966
hg1911966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516111
Samples
Known GenesGTPBP6, PLCXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972055
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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