A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464085



Internal ID21121638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104554532..104609537hg38UCSC Ensembl
chr12:104948310..105003315hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3855006
hg1955006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995919
Samples
Known GenesCHST11, MIR3922
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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