A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560886



Internal ID20933957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106498887..106499151hg38UCSC Ensembl
chr6:106946762..106947026hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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