A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443405



Internal ID22109588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97852676..97852676hg38UCSC Ensembl
chr13:98504930..98504930hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760391
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443405
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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