A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460898



Internal ID21118451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65896647..65942502hg38UCSC Ensembl
chr12:66290427..66336282hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3845856
hg1945856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003028
Samples
Known GenesHMGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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