A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469785



Internal ID21127338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92415927..92426513hg38UCSC Ensembl
chr12:92809703..92820289hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3810587
hg1910587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005761
Samples
Known GenesCLLU1, CLLU1OS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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