A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566166



Internal ID20939237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105724605..105725123hg38UCSC Ensembl
chr6:106172480..106172998hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566166
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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