A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766594



Internal ID20542454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154424921..154425042hg38UCSC Ensembl
chrX:153653264..153653385hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285681
Samples
Known GenesLOC158960
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766594
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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