A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744211



Internal ID20520208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24709083..24709083hg38UCSC Ensembl
chrX:24727200..24727200hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277586
Samples
Known GenesPOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744211
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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