A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580484



Internal ID20953555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47191476..47192367hg38UCSC Ensembl
chr17:45268842..45269733hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580484
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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