A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443126



Internal ID22109310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87867901..87867901hg38UCSC Ensembl
chr9:90482816..90482816hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767415
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443126
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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