A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290792



Internal ID20500010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48728779..48728779hg38UCSC Ensembl
chrX:48587184..48587184hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290792
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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