A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649195



Internal ID21841242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107274232..107274295hg38UCSC Ensembl
chrX:106517462..106517525hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649195
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