A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268882



Internal ID20478100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8978445..8978445hg38UCSC Ensembl
chrX:8946486..8946486hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268882
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