A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438999



Internal ID22105176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32693949..32693949hg38UCSC Ensembl
chr9:32693947..32693947hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765490
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438999
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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