A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553786



Internal ID20926899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84597946..84598220hg38UCSC Ensembl
chr2:84825070..84825344hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259105
Samples
Known GenesDNAH6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553786
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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