A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458918



Internal ID21116471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77036585..77040608hg38UCSC Ensembl
chr12:77430365..77434388hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg384024
hg194024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004135
Samples
Known GenesE2F7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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