A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460487



Internal ID22518370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49194220..49200910hg38UCSC Ensembl
chr11:49215772..49222462hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg386691
hg196691
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853802
Supporting Variants
Samples
Known GenesFOLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460487
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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