A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831052



Internal ID22605987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9784257..9786400hg38UCSC Ensembl
chr1:9844315..9846458hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482515
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831052
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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