A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481772



Internal ID21139325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26268653..26271839hg38UCSC Ensembl
chr13:26842790..26845976hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg383187
hg193187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007453
Samples
Known GenesCDK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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