A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439326



Internal ID22105503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3634954..3634954hg38UCSC Ensembl
chr6:3635188..3635188hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764290
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439326
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