A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446961



Internal ID22113138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73690969..73690969hg38UCSC Ensembl
chr15:73983310..73983310hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15755868
Samples
Known GenesCD276
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446961
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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