A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441632



Internal ID22107813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19326706..19326706hg38UCSC Ensembl
chr19:19437515..19437515hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756506
Samples
Known GenesMAU2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441632
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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