A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934776



Internal ID21354847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107418230..107418230hg38UCSC Ensembl
chrX:106661460..106661460hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15206051
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934776
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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