A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262411



Internal ID20471629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47148605..47148665hg38UCSC Ensembl
chrX:47008004..47008064hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768231
Supporting Variants
Samples
Known GenesRBM10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262411
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