A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668966



Internal ID21617271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150382868..150383203hg38UCSC Ensembl
chrX:149551136..149551471hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165953
SamplesHG00513
Known GenesMAMLD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668966
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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