A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522493



Internal ID20895854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46970333..46974459hg38UCSC Ensembl
chr17:45047699..45051825hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg384127
hg194127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035952
Samples
Known GenesMIR5089
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522493
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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