A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165116



Internal ID21484968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120582002..120582062hg38UCSC Ensembl
chrX:119715857..119715917hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671790
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165116
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