A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767113



Internal ID20542973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80809711..80809775hg38UCSC Ensembl
chrX:80065210..80065274hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289551
Samples
Known GenesBRWD3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767113
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