A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559328



Internal ID20932399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111319398..111320193hg38UCSC Ensembl
chr6:111640601..111641396hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268489
Samples
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559328
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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