A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470243



Internal ID21127796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102329463..102330321hg38UCSC Ensembl
chr12:102723241..102724099hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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