A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738182



Internal ID20514149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:83878171..83878171hg38UCSC Ensembl
chrX:83133179..83133179hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381352
hg191352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295373
Samples
Known GenesCYLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738182
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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