A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517841



Internal ID20891202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50767900..50808786hg38UCSC Ensembl
chr17:48845261..48886147hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3840887
hg1940887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187202
Samples
Known GenesMIR8059
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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