A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766090



Internal ID22100562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45633174..45633174hg38UCSC Ensembl
chr21:47053088..47053088hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766090
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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