A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465694



Internal ID21123247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10923438..10933265hg38UCSC Ensembl
chr12:11076037..11085864hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg389828
hg199828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996255
Samples
Known GenesPRH1-PRR4, PRH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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