A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050173



Internal ID21959407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115436030..115436030hg38UCSC Ensembl
chrX:114670492..114670492hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050173
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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