A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930193



Internal ID21350262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87205391..87205391hg38UCSC Ensembl
chrX:86460394..86460394hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15206133
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930193
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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