A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466698



Internal ID21124251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50215739..50218103hg38UCSC Ensembl
chr12:50609522..50611886hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg382365
hg192365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001240
Samples
Known GenesLIMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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