A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510783



Internal ID20884106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53158401..53159137hg38UCSC Ensembl
chr15:53450598..53451334hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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