A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290104



Internal ID20499322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103200601..103200669hg38UCSC Ensembl
chr10:104960358..104960426hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290104
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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