A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754068



Internal ID20529928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85088046..85088132hg38UCSC Ensembl
chrX:84343052..84343138hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291213
Samples
Known GenesAPOOL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754068
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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