A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514036



Internal ID20887386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24792769..24843570hg38UCSC Ensembl
chr15:25037916..25088717hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3850802
hg1950802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022569
Samples
Known GenesSNRPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514036
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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