A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750387



Internal ID20526402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46275709..46275837hg38UCSC Ensembl
chrX:46135144..46135272hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750387
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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