A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496480



Internal ID20869682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25085405..25086669hg38UCSC Ensembl
chr15:25330552..25331816hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381265
hg191265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022602
Samples
Known GenesSNORD116-17, SNORD116-18, SNORD116-19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496480
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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