A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515231



Internal ID20888590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90103089..90218641hg38UCSC Ensembl
chr15:90646321..90761873hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38115553
hg19115553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177260
Samples
Known GenesSEMA4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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