A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828489



Internal ID22603424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192651866..192670331hg38UCSC Ensembl
chr1:192620996..192639461hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3818466
hg1918466
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465537
Samples
Known GenesRGS13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828489
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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