A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465555



Internal ID21123108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50113338..50117745hg38UCSC Ensembl
chr12:50507121..50511528hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg384408
hg194408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001230
Samples
Known GenesCOX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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