A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565889



Internal ID20938960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136865411..136865670hg38UCSC Ensembl
chr6:137186549..137186808hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272413
Samples
Known GenesPEX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565889
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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