A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760302



Internal ID20536162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78780159..78795082hg38UCSC Ensembl
chrX:78035656..78050579hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3814924
hg1914924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760302
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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