A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957732



Internal ID22732843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204034282..204034282hg38UCSC Ensembl
chr1:204003410..204003410hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351579
Samples
Known GenesLINC00303
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957732
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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