A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346105



Internal ID21003658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105356482..105369207hg38UCSC Ensembl
chr2:105972939..105985664hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3812726
hg1912726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205812
Samples
Known GenesFHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346105
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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