A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456146



Internal ID21113699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25898835..25900589hg38UCSC Ensembl
chr12:26051768..26053522hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381755
hg191755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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