A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507286



Internal ID20880574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44819101..44889200hg38UCSC Ensembl
chr15:45111299..45181398hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3870100
hg1970100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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