A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468343



Internal ID21125896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73520907..73521225hg38UCSC Ensembl
chr12:73914687..73915005hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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