A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570790



Internal ID20943861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135978814..136004461hg38UCSC Ensembl
chr6:136299952..136325599hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3825648
hg1925648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272376
Samples
Known GenesPDE7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570790
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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