A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501371



Internal ID20874604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15698201..15708700hg38UCSC Ensembl
chr17:15601515..15612014hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181349
Samples
Known GenesZNF286A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501371
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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