A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495839



Internal ID20869034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95684986..95695304hg38UCSC Ensembl
chr15:96228215..96238533hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3810319
hg1910319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495839
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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