A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537229



Internal ID20910568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177686334..177686978hg38UCSC Ensembl
chr2:178551062..178551706hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256219
Samples
Known GenesPDE11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537229
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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