A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048598



Internal ID21957831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13755075..13755075hg38UCSC Ensembl
chrX:13773194..13773194hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642786
Samples
Known GenesOFD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048598
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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