A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736080



Internal ID20512025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18334634..18334634hg38UCSC Ensembl
chrX:18352754..18352754hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg385969
hg195969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275529
Samples
Known GenesSCML2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736080
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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