A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847903



Internal ID22622838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40290210..40292984hg38UCSC Ensembl
chr12:40684012..40686786hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382775
hg192775
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453190
Samples
Known GenesLRRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847903
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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