A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490647



Internal ID21148200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114271400..114271775hg38UCSC Ensembl
chr13:115036875..115037250hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007833
Samples
Known GenesCDC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490647
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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