A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578588



Internal ID20951659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58881536..58883189hg38UCSC Ensembl
chr17:56958897..56960550hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381654
hg191654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243686
Samples
Known GenesPPM1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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