A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738109



Internal ID20514076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35692327..35692327hg38UCSC Ensembl
chrX:35710444..35710444hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738109
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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