A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441761



Internal ID22107942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35527100..35527100hg38UCSC Ensembl
chr19:36018002..36018002hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759527
Samples
Known GenesSBSN
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441761
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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