A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164878



Internal ID21450001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107662934..107662934hg38UCSC Ensembl
chrX:106906164..106906164hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621442
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164878
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