A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592541



Internal ID20965612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49656989..49657572hg38UCSC Ensembl
chr17:47734351..47734934hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245148
Samples
Known GenesSPOP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592541
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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