A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853907



Internal ID22628842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124749048..124751920hg38UCSC Ensembl
chr9:127511327..127514199hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg382873
hg192873
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511331
Samples
Known GenesNR6A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853907
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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