A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467145



Internal ID21124698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93518881..93521031hg38UCSC Ensembl
chr12:93912657..93914807hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382151
hg192151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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