A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166947



Internal ID21411197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26194092..26194217hg38UCSC Ensembl
chrX:26212209..26212334hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670872
Supporting Variants
SamplesHG00513
Known GenesMAGEB6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166947
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