A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585764



Internal ID20958835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44751113..44754441hg38UCSC Ensembl
chr17:42828481..42831809hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg383329
hg193329
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242340
Samples
Known GenesDBF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585764
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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