A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505691



Internal ID20878964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50759675..50763830hg38UCSC Ensembl
chr15:51051872..51056027hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg384156
hg194156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181117
Samples
Known GenesSPPL2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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