A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465672



Internal ID21123225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13666934..13667308hg38UCSC Ensembl
chr12:13819868..13820242hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999476
Samples
Known GenesGRIN2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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