A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969839



Internal ID22744774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54031683..54041182hg38UCSC Ensembl
chrX:54058116..54067615hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516374
Samples
Known GenesPHF8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969839
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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