A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469362



Internal ID21126915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22565923..22569031hg38UCSC Ensembl
chr12:22718857..22721965hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg383109
hg193109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998349
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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