A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761895



Internal ID22096397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58309453..58309453hg38UCSC Ensembl
chr20:56884509..56884509hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4443966
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761895
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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