A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938802



Internal ID21358871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9388955..9388955hg38UCSC Ensembl
chrX:9356995..9356995hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205539
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938802
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer