A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438034



Internal ID22104215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52269161..52269161hg38UCSC Ensembl
chr12:52662945..52662945hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756063
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438034
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