A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237002



Internal ID20804043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49179806..49863338hg38UCSC Ensembl
chr11:49201358..49884890hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38683533
hg19683533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585658
Supporting Variants
Samples
Known GenesFOLH1, LOC440040
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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