A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456594



Internal ID21114147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45484798..45499715hg38UCSC Ensembl
chr12:45878581..45893498hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3814918
hg1914918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456594
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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