A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286744



Internal ID20495962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73109735..73123385hg38UCSC Ensembl
chrX:72329574..72343224hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3813651
hg1913651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286744
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