A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768053



Internal ID20543913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153605516..153605573hg38UCSC Ensembl
chrX:152870971..152871028hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768053
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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