A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512011



Internal ID20885341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17053210..17057043hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512011
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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