A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499606



Internal ID20872827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41445229..41449130hg38UCSC Ensembl
chr15:41737427..41741328hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023886
Samples
Known GenesRTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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