A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472698



Internal ID21130251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77122949..77123750hg38UCSC Ensembl
chr12:77516729..77517530hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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