A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15760567



Internal ID22095053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142241820..142241820hg38UCSC Ensembl
chr8:143323181..143323181hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4438370
Supporting Variants
Samples
Known GenesTSNARE1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15760567
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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