A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940455



Internal ID21360524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23002080..23002080hg38UCSC Ensembl
chrX:23020197..23020197hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205983
SamplesHG002
Known GenesDDX53, LOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940455
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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