A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292628



Internal ID20501846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78650931..78655345hg38UCSC Ensembl
chrX:77906428..77910842hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg384415
hg194415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292628
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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