A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974812



Internal ID22749747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133105933..133112512hg38UCSC Ensembl
chrX:132239961..132246540hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg386580
hg196580
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974812
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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