A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506217



Internal ID20879495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39887601..39893900hg38UCSC Ensembl
chr15:40179802..40186101hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182435
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506217
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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