A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481525



Internal ID21139078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112397688..112403373hg38UCSC Ensembl
chr12:112835492..112841177hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg385686
hg195686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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