A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542709



Internal ID20915967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177627073..177627789hg38UCSC Ensembl
chr2:178491801..178492517hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256217
Samples
Known GenesPDE11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542709
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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