A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446876



Internal ID22113053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99549037..99549037hg38UCSC Ensembl
chr7:99146660..99146660hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765931
Samples
Known GenesFAM200A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446876
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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