A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578528



Internal ID20951599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48963559..49823161hg38UCSC Ensembl
chr11:48985111..49844713hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38859603
hg19859603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1095n223
Supporting Variantsnssv18236215
Samples
Known GenesFOLH1, LOC440040, TRIM49B, TRIM64C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578528
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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