A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440204



Internal ID22106382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170319647..170319647hg38UCSC Ensembl
chr3:170037435..170037435hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758226
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440204
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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