A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611183



Internal ID21559488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115191439..115191439hg38UCSC Ensembl
chrX:114426002..114426002hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164734
SamplesHG03009
Known GenesLRCH2, RBMXL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611183
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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