A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288984



Internal ID20498202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3691429..3691484hg38UCSC Ensembl
chrX:3609470..3609525hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765898
Supporting Variants
Samples
Known GenesPRKX
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288984
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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