A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460801



Internal ID21118354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39969598..39972147hg38UCSC Ensembl
chr12:40363400..40365949hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999046
Samples
Known GenesSLC2A13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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