A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972533



Internal ID22747468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122645286..122654163hg38UCSC Ensembl
chrX:121779139..121788016hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg388878
hg198878
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972533
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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