A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438894



Internal ID22105071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39247470..39247470hg38UCSC Ensembl
chr3:39288961..39288961hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760021
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438894
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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