A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444578



Internal ID22110758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122419595..122419921hg38UCSC Ensembl
chr3:122138442..122138768hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766856
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444578
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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