A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761487



Internal ID22095980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86215788..86215788hg38UCSC Ensembl
chr3:86264938..86264938hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg383653
hg193653
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4439482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761487
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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