A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564449



Internal ID20937520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43194338..43194856hg38UCSC Ensembl
chr6:43162076..43162594hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271337
Samples
Known GenesCUL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564449
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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