A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100882



Internal ID22010115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:81367737..81367796hg38UCSC Ensembl
chrX:80623236..80623295hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100882
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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