A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577486



Internal ID20950557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72998278..72999600hg38UCSC Ensembl
chr11:72709323..72710645hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226497
Samples
Known GenesFCHSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577486
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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