A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747869



Internal ID20523891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43715669..43715669hg38UCSC Ensembl
chrX:43574916..43574916hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282420
Samples
Known GenesMAOA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747869
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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