A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589684



Internal ID20962755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42890706..42892634hg38UCSC Ensembl
chr17:41042723..41044651hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381929
hg191929
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242262
Samples
Known GenesLINC00671
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589684
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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