A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765227



Internal ID20541087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112843485..112843565hg38UCSC Ensembl
chrX:112086713..112086793hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765227
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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