A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587583



Internal ID20960654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73581799..73582277hg38UCSC Ensembl
chr11:73292844..73293322hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226678
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587583
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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