A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511831



Internal ID20885161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24198001..24213000hg38UCSC Ensembl
chr15:24443148..24458147hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3815000
hg1915000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511831
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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