A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486057



Internal ID21143610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110126098..110141314hg38UCSC Ensembl
chr12:110563903..110579119hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3815217
hg1915217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996898
Samples
Known GenesIFT81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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