A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588375



Internal ID20961446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43184373..43185101hg38UCSC Ensembl
chr17:41336390..41337118hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242278
Samples
Known GenesNBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588375
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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