A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442999



Internal ID22109182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10984536..10984536hg38UCSC Ensembl
chr5:10984648..10984648hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758910
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442999
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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