A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470146



Internal ID21127699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40289001..40290700hg38UCSC Ensembl
chr12:40682803..40684502hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1521n223
Supporting Variantsnssv17999076
Samples
Known GenesLRRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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