A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761900



Internal ID22096402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62291818..62291818hg38UCSC Ensembl
chr20:60866874..60866874hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444132
Supporting Variants
Samples
Known GenesOSBPL2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761900
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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