A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345114



Internal ID21002667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175071506..175091812hg38UCSC Ensembl
chr2:175936234..175956540hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3820307
hg1920307
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207437
Samples
Known GenesATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345114
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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