A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931016



Internal ID21351085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1293845..1293845hg38UCSC Ensembl
chrX:1412738..1412738hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205196
SamplesHG002
Known GenesCSF2RA
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931016
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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