A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742739



Internal ID20518724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93441683..93441683hg38UCSC Ensembl
chrX:92696682..92696682hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742739
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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