A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467558



Internal ID21125111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70085201..70090100hg38UCSC Ensembl
chr12:70478981..70483880hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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