A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761406



Internal ID22095897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126013136..126013303hg38UCSC Ensembl
chr9:128775415..128775582hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761406
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