A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464346



Internal ID21121899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87270060..87353114hg38UCSC Ensembl
chr12:87663837..87746891hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg3883055
hg1983055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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