A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165733



Internal ID21480805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137439009..137440319hg38UCSC Ensembl
chrX:136521168..136522478hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg381311
hg191311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669902
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165733
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