A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448383



Internal ID22114561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165892146..165892146hg38UCSC Ensembl
chr1:165861383..165861383hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg382355
hg192355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760461
Samples
Known GenesUCK2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448383
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