A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15756117



Internal ID22090600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81793471..81793471hg38UCSC Ensembl
chr9:84408386..84408386hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4443355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15756117
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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