A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804189



Internal ID21249527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31591654..31592058hg38UCSC Ensembl
chr22:31987640..31988044hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681508
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804189
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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