A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564455



Internal ID20937526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150093047..150093784hg38UCSC Ensembl
chr5:149472610..149473347hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5985n223
Supporting Variantsnssv18268691
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564455
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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