A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761006



Internal ID22095496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23267991..23267991hg38UCSC Ensembl
chr20:23248628..23248628hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4442566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761006
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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