A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459326



Internal ID21116879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92565634..92566078hg38UCSC Ensembl
chr12:92959410..92959854hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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