A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336466



Internal ID20994019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222453411..222453930hg38UCSC Ensembl
chr2:223318130..223318649hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086930
Samples
Known GenesSGPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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