A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497028



Internal ID20870231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68928601..68931000hg38UCSC Ensembl
chr15:69220940..69223339hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195135
Samples
Known GenesMIR548H4, NOX5, SPESP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497028
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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