A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572711



Internal ID20945782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17645461..17894090hg38UCSC Ensembl
chr6:17645692..17894321hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38248630
hg19248630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270602
Samples
Known GenesKIF13A, NUP153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572711
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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