A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437350



Internal ID22103529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97410945..97411057hg38UCSC Ensembl
chr9:100173227..100173339hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761082
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437350
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