A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466561



Internal ID21124114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103984918..103985600hg38UCSC Ensembl
chr12:104378696..104379378hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995676
Samples
Known GenesTDG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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