A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509996



Internal ID20883309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90301191..90410396hg38UCSC Ensembl
chr15:90844423..90953628hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38109206
hg19109206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178789
Samples
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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