A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828859



Internal ID22603794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201963595..201966694hg38UCSC Ensembl
chr1:201932723..201935822hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452694
Samples
Known GenesTIMM17A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828859
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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