A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460374



Internal ID21117927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2985823..2986512hg38UCSC Ensembl
chr12:3094989..3095678hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998881
Samples
Known GenesTEAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460374
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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