A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465897



Internal ID22523787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56727378..56796579hg38UCSC Ensembl
chr11:56494854..56564055hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3869202
hg1969202
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863023
Supporting Variants
Samples
Known GenesMIR6128, OR9G4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465897
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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