A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437994



Internal ID22104175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50414371..50414371hg38UCSC Ensembl
chr16:50448282..50448282hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766160
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437994
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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