A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583368



Internal ID20956439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30098005..30098459hg38UCSC Ensembl
chr17:28425023..28425477hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3071n223
Supporting Variantsnssv18241745
Samples
Known GenesEFCAB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583368
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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