A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339085



Internal ID20996638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:169720853..169731149hg38UCSC Ensembl
chr2:170577363..170587659hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3810297
hg1910297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079981
Samples
Known GenesPHOSPHO2-KLHL23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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