A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048779



Internal ID21958014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40622209..40622209hg38UCSC Ensembl
chrX:40481461..40481461hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048779
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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