A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801062



Internal ID21246402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171210718..171210799hg38UCSC Ensembl
chr1:171179857..171179938hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13700576
Samples
Known GenesFMO2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801062
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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