A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437299



Internal ID22103478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170774321..170774321hg38UCSC Ensembl
chr5:170201325..170201325hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757337
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437299
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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