A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975908



Internal ID22750843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54036583..54045356hg38UCSC Ensembl
chrX:54063016..54071789hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg388774
hg198774
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516375
Samples
Known GenesPHF8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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