A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455982



Internal ID21113535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107429468..107429839hg38UCSC Ensembl
chr12:107823245..107823616hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996158
Samples
Known GenesBTBD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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