A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234472



Internal ID20801512
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 StatusS
Merged Variantsnsv6576832
Supporting Variants
Samples
Known GenesFOLH1, LOC440040
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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