A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443749



Internal ID22109930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109524283..109524406hg38UCSC Ensembl
chr9:112286563..112286686hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763171
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SUBSINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443749
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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