A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466226



Internal ID21123779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77390071..77390429hg38UCSC Ensembl
chr12:77783851..77784209hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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