A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461593



Internal ID21119146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101464033..101475981hg38UCSC Ensembl
chr12:101857811..101869759hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3811949
hg1911949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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