A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498784



Internal ID20871997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90245215..90246012hg38UCSC Ensembl
chr15:90788447..90789244hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191286
Samples
Known GenesCIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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