A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512791



Internal ID20886129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24997155..25001097hg38UCSC Ensembl
chr15:25242302..25246244hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383943
hg193943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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