A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925733



Internal ID21345807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180859067..180859067hg38UCSC Ensembl
chr1:180828203..180828203hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188869
SamplesHG002
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925733
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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