A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595281



Internal ID20968352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77825720..77826353hg38UCSC Ensembl
chr11:77536766..77537399hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1233n223
Supporting Variantsnssv18226377
Samples
Known GenesAAMDC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595281
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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