A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514871



Internal ID20888226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90836998..90850296hg38UCSC Ensembl
chr15:91380228..91393526hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3813299
hg1913299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514871
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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