A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511093



Internal ID20884418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76459753..76466913hg38UCSC Ensembl
chr15:76752094..76759254hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg387161
hg197161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025779
Samples
Known GenesSCAPER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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