A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446604



Internal ID22112782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69182888..69182888hg38UCSC Ensembl
chr11:68950356..68950356hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761635
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446604
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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