A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828369



Internal ID22603304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158356188..158358395hg38UCSC Ensembl
chr1:158325978..158328185hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382208
hg192208
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452542
Samples
Known GenesCD1E
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828369
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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