A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566687



Internal ID20939758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110886036..110886425hg38UCSC Ensembl
chr6:111207239..111207628hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268452
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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