A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563403



Internal ID20936474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117335679..117336191hg38UCSC Ensembl
chr6:117656842..117657354hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268588
Samples
Known GenesROS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563403
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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