A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765931



Internal ID22100402
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 StatusS
Merged Variantsnsv4446876
Supporting Variants
Samples
Known GenesFAM200A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765931
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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