A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283071



Internal ID20492289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94330116..94330508hg38UCSC Ensembl
chrX:93585115..93585507hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283071
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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