A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766067



Internal ID22100539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11009487..11009487hg38UCSC Ensembl
chr20:10990135..10990135hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4442728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766067
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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