A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576832



Internal ID20949903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49182705..49862910hg38UCSC Ensembl
chr11:49204257..49884462hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38680206
hg19680206
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1095n223
Supporting Variantsnssv18234472
Samples
Known GenesFOLH1, LOC440040
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576832
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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