A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046886



Internal ID21956119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9338344..9338344hg38UCSC Ensembl
chrX:9306384..9306384hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046886
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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