A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196032



Internal ID20763072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49197675..49199519hg38UCSC Ensembl
chr11:49219227..49221071hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381845
hg191845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466135
Supporting Variants
Samples
Known GenesFOLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196032
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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