A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583237



Internal ID20956308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17424053..17489185hg38UCSC Ensembl
chr17:17327367..17392499hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3865133
hg1965133
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242086
Samples
Known GenesMED9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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