A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050787



Internal ID21960020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147378088..147378088hg38UCSC Ensembl
chrX:146459606..146459606hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg381353
hg191353
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050787
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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