A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514115



Internal ID20887467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8092093..8099704hg38UCSC Ensembl
chr17:7995411..8003022hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387612
hg197612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186704
Samples
Known GenesALOXE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514115
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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