A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447226



Internal ID22113403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38110041..38110041hg38UCSC Ensembl
chr22:38506048..38506048hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381613
hg191613
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765604
Samples
Known GenesBAIAP2L2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447226
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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