A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047386



Internal ID21956620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119208353..119208353hg38UCSC Ensembl
chrX:118342316..118342316hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047386
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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