A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559823



Internal ID20932894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11549660..11550342hg38UCSC Ensembl
chr6:11549893..11550575hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268569
Samples
Known GenesTMEM170B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559823
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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