A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509725



Internal ID20883036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74881105..74894639hg38UCSC Ensembl
chr15:75173446..75186980hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3813535
hg1913535
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185183
Samples
Known GenesMPI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509725
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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