A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804228



Internal ID21249566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43834657..43834936hg38UCSC Ensembl
chr22:44230537..44230816hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678614
Samples
Known GenesSULT4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804228
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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