A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832491



Internal ID22607426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213564052..213567201hg38UCSC Ensembl
chr2:214428776..214431925hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482623
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832491
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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