A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463112



Internal ID21120665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52029391..52032110hg38UCSC Ensembl
chr12:52423175..52425894hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg382720
hg192720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001375
Samples
Known GenesNR4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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