A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469588



Internal ID21127141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101860981..101874344hg38UCSC Ensembl
chr12:102254759..102268122hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3813364
hg1913364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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