A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464696



Internal ID21122249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98310744..98322056hg38UCSC Ensembl
chr12:98704522..98715834hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3811313
hg1911313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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