A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578767



Internal ID20951838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46578883..46579756hg38UCSC Ensembl
chr11:46600433..46601306hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219991
Samples
Known GenesAMBRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578767
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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