A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971006



Internal ID22745941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105108324..105121364hg38UCSC Ensembl
chrX:104353006..104366046hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3813041
hg1913041
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515082
Samples
Known GenesIL1RAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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