A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165604



Internal ID21492932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125503301..125503301hg38UCSC Ensembl
chrX:124637150..124637150hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381236
hg191236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607198
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165604
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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