A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465137



Internal ID21122690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96689801..96697800hg38UCSC Ensembl
chr12:97083579..97091578hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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