A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706131



Internal ID21227926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101900286..101900337hg38UCSC Ensembl
chrX:101155259..101155310hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818342
Supporting Variants
Samples
Known GenesZMAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706131
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.59375


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