A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736616



Internal ID20512567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4117501..4117501hg38UCSC Ensembl
chrX:4035542..4035542hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736616
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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