A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836988



Internal ID22611923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64547319..64550418hg38UCSC Ensembl
chr3:64532995..64536094hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1460n209
Supporting Variantsnssv17494039
Samples
Known GenesADAMTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836988
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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