A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578245



Internal ID20951316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40277446..40277978hg38UCSC Ensembl
chr17:38433698..38434230hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242948
Samples
Known GenesWIPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578245
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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