A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448684



Internal ID22114861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77586721..77586721hg38UCSC Ensembl
chr5:76882546..76882546hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756017
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448684
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer