A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828668



Internal ID22603603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183849456..183857281hg38UCSC Ensembl
chr1:183818590..183826415hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg387826
hg197826
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464154
Samples
Known GenesRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828668
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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