A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280724



Internal ID20489942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103892093..103897752hg38UCSC Ensembl
chrX:103147014..103152673hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752717
Supporting Variants
Samples
Known GenesMIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280724
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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