A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765666



Internal ID22100146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95751361..95751361hg38UCSC Ensembl
chr9:98513643..98513643hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4443272
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765666
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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